http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#head
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#assertion
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#provenance
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#assertion
http://rdf.disgenet.org/resource/gda/DGNcaf5666e91b7fc9cf5dc65588f5f2a72
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/1967
http://rdf.disgenet.org/resource/gda/DGNcaf5666e91b7fc9cf5dc65588f5f2a72
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C1858991
http://rdf.disgenet.org/resource/gda/DGNcaf5666e91b7fc9cf5dc65588f5f2a72
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#provenance
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#assertion
http://purl.org/dc/terms/description
[Leukoencephalopathy with vanishing white matter (VWM), also called childhood ataxia with central nervous system hypomyelination (CACH), is an autosomal recessive disease caused by mutations in any of the five genes encoding subunits of the eukaryotic translation initiation factor eIF2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#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/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/16823698
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#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/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/dc/terms/created
2017-10-17T13:12:16+02:00
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP328937.RA-g0KmiuIj5riE0SOxNHd8hLgyecgkPRhbY3CwK99BSE
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