http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#head
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#provenance
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://rdf.disgenet.org/resource/gda/DGNb5c17f2046cb3f8423be5a96b8e360ab
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4566
http://rdf.disgenet.org/resource/gda/DGNb5c17f2046cb3f8423be5a96b8e360ab
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0023264
http://rdf.disgenet.org/resource/gda/DGNb5c17f2046cb3f8423be5a96b8e360ab
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#provenance
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://purl.org/dc/terms/description
[To investigate the spectrum of common mitochondrial mutations in Northern China during the years of 2000-2005, 552 patients of mitochondrial encephalomyopathies clinically diagnosed as MELAS, MERRF or Leigh's syndrome, 14 cases of LHON and 46 cases of aminoglycoside induced deafness along with their family members, accepted routine point mutation tests at nucleotide positions 3243, 8344, 8993, 11778 or 1555 in mitochondrial genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://purl.org/ontology/wi/core#evidence
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/17276742
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#assertion
http://www.w3.org/ns/prov#wasGeneratedBy
http://purl.obolibrary.org/obo/ECO_0000203
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://purl.org/pav/importedOn
2017-02-19
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.obolibrary.org/obo/ECO_0000212
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#comment
Gene-disease associations inferred from text-mining the literature.
http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature
http://www.w3.org/2000/01/rdf-schema#label
DisGeNET evidence - LITERATURE
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/dc/terms/created
2017-10-17T13:14:49+02:00
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP727925.RAAZD48lnAj3YhEaAYeZ2gsGUXimyX0XLQD0MzTgh4ZBI
http://purl.org/pav/version
v5.0.0.0
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://purl.org/pav/version
v5.0.0