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