http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#head http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#assertion http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#provenance http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#assertion http://rdf.disgenet.org/resource/gda/DGNd81514f3effc66f9d3c216b80d4535c7 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/8398 http://rdf.disgenet.org/resource/gda/DGNd81514f3effc66f9d3c216b80d4535c7 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C2931845 http://rdf.disgenet.org/resource/gda/DGNd81514f3effc66f9d3c216b80d4535c7 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#provenance http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#assertion http://purl.org/dc/terms/description [More recently, it was found that mutations in the PLA2G6 gene cause both infantile neuroaxonal dystrophy (INAD) and, more rarely, an atypical neuroaxonal dystrophy that overlaps clinically with other forms of NBIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#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/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18981035 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#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/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/dc/terms/created 2017-10-17T13:17:28+02:00 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1143679.RAwUwlIgeTBPzPwCN6ezzyZa89jNqT1ZvxxXw27IXVgcE 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