@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:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_head { this: np:hasAssertion dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_assertion; np:hasProvenance dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_provenance; np:hasPublicationInfo dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_publicationInfo; a np:Nanopublication . dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_assertion a np:Assertion . dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_provenance a np:Provenance . dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_publicationInfo a np:PublicationInfo . } dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_assertion { miriam-gene:19 a ncit:C16612 . lld:C0038454 a ncit:C7057 . dgn-gda:DGN76c3bc5b349d49be7ff7d2d0b3fdf9c8 sio:SIO_000628 miriam-gene:19, lld:C0038454; a sio:SIO_001122 . } dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_provenance { dgn-np:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_assertion dcterms:description "[Genotypes for ABCA1, IRAK1, and ROS1 may prove useful for assessment of the genetic risk for atherothrombotic cerebral infarction, whereas those for LIMK1 and CYP3A4 may be similarly beneficial in assessment of the genetic risk for intracerebral hemorrhage and subarachnoid hemorrhage, respectively.]. 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:18566305; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP110422.RAnSa8r23PLiN2OI6pORPzdfk1ZFluDMin7fbGhYL2wdM130_publicationInfo { this: dcterms:created "2015-08-25T14:38:41+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" . }