http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#head
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#assertion
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#provenance
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#assertion
http://rdf.disgenet.org/resource/gda/DGN439d75a0bb3a22315e7b9b1480c6d546
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/5071
http://rdf.disgenet.org/resource/gda/DGN439d75a0bb3a22315e7b9b1480c6d546
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C4275179
http://rdf.disgenet.org/resource/gda/DGN439d75a0bb3a22315e7b9b1480c6d546
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#provenance
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#assertion
http://purl.org/dc/terms/description
[Our data suggest that compound heterozygous mutations (EX 3 and EX 3_4 del) in the parkin gene were the cause of EOPD in one of six Caucasian families; heterozygous EX 3 del and heterozygous EX 3_4 del forms were insufficient to cause this disorder, consistent with a loss-of-function mechanism of the parkin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#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/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18068301
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#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/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/dc/terms/created
2017-10-17T13:15:11+02:00
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP786446.RAGFxi832q0k14dUM-qnx-6GqWJa6fWyooCyM-zGSOlr0
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