@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:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_head { this: np:hasAssertion dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_assertion; np:hasProvenance dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_provenance; np:hasPublicationInfo dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_publicationInfo; a np:Nanopublication . dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_assertion a np:Assertion . dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_provenance a np:Provenance . dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_publicationInfo a np:PublicationInfo . } dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_assertion { miriam-gene:203228 a ncit:C16612 . lld:C0751072 a ncit:C7057 . dgn-gda:DGNd31c8833c53a3a504501afe39d525868 sio:SIO_000628 miriam-gene:203228, lld:C0751072; a sio:SIO_001121 . } dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_provenance { dgn-np:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_assertion dcterms:description "[Finally, we discuss the issues surrounding accurate clinical and technological diagnosis of patients with FTLD and/or ALS associated with the C9ORF72 expansion, and outline areas for future research that might aid better diagnosis and genetic counselling of patients with seemingly sporadic or familial FTLD or ALS and their relatives.]. 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:24515836; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP979971.RA-VyTplsHjXPO9GKywiL4_IOcowdu1NDjP2EufwizVhI130_publicationInfo { this: dcterms:created "2015-08-25T14:47:38+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }