@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_head { this: np:hasAssertion dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_assertion; np:hasProvenance dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_provenance; np:hasPublicationInfo dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_publicationInfo; a np:Nanopublication . dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_assertion a np:Assertion . dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_provenance a np:Provenance . dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_publicationInfo a np:PublicationInfo . } dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_assertion { miriam-gene:23435 a ncit:C16612 . lld:C1862939 a ncit:C7057 . dgn-gda:DGN3a118b1782b9e5a31254288b07ce3e26 sio:SIO_000628 miriam-gene:23435, lld:C1862939; a sio:SIO_001121 . } dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_provenance { dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_assertion dcterms:description "[This study defined the distribution and frequency of mutations of FALS in a Taiwanese Han Chinese population, which not only broadens the spectrum of the mutations causing FALS, but also further highlights the importance of FUS and TARDBP in the pathogenesis of amyotrophic lateral sclerosis (ALS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:20472325; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP812307.RACJwtrgrMg4WhSjeuQCywfnNVBCQsgogbO5ToySlnNW0130_publicationInfo { this: dcterms:created "2016-05-13T12:47:53+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }