@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:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_head { this: np:hasAssertion dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_assertion; np:hasProvenance dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_provenance; np:hasPublicationInfo dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_publicationInfo; a np:Nanopublication . dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_assertion a np:Assertion . dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_provenance a np:Provenance . dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_assertion { miriam-gene:6647 a ncit:C16612 . lld:C1862939 a ncit:C7057 . dgn-gda:DGN85c51ca02f45b10f00da131ca369ad49 sio:SIO_000628 miriam-gene:6647, lld:C1862939; a sio:SIO_001121 . } dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_provenance { dgn-np:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_assertion dcterms:description "[These studies show that, in addition to the previously demonstrated histological and electromyographic deficits, this transgenic mouse also presents changes in motor function reminiscent of the human disease, reinforcing and extending its validity as an animal model of familial amyotrophic lateral sclerosis (FALS) and allowing the investigation of novel drug treatment for 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:9376520; 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:NP1384316.RANaHMvB8FXP1NZE6YxSRt922rTu7d89kNuH_FPt00U1Y130_publicationInfo { this: dcterms:created "2016-05-13T12:52:13+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" . }