@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:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_head { this: np:hasAssertion dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_assertion; np:hasProvenance dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_provenance; np:hasPublicationInfo dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_publicationInfo; a np:Nanopublication . dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_assertion a np:Assertion . dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_provenance a np:Provenance . dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_assertion { miriam-gene:9856 a ncit:C16612 . lld:C0266463 a ncit:C7057 . dgn-gda:DGNc82d79dc37b4be906f3e48d99b4a2137 sio:SIO_000628 miriam-gene:9856, lld:C0266463; a sio:SIO_001121 . } dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_provenance { dgn-np:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_assertion dcterms:description "[LIS1 was the first gene cloned that was important for neuronal migration in any organism, and heterozygous mutations or deletions of LIS1 are found in the majority of patients with lissencephaly, while DCX mutations were found in males with X-linked lissencephaly.]. 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:20688183; 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:NP831058.RA9yVENt3-LiuyDLHfC3h75F-TTCkwc9LG8ME_68jX8_Y130_publicationInfo { this: dcterms:created "2016-05-13T12:48:01+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" . }