@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:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_head { this: np:hasAssertion dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_assertion; np:hasProvenance dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_provenance; np:hasPublicationInfo dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_publicationInfo; a np:Nanopublication . dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_assertion a np:Assertion . dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_provenance a np:Provenance . dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_publicationInfo a np:PublicationInfo . } dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_assertion { miriam-gene:79001 a ncit:C16612 . lld:C0750384 a ncit:C7057 . dgn-gda:DGNf175e5c2a8adf881849496184aea3dfa sio:SIO_000628 miriam-gene:79001, lld:C0750384; a sio:SIO_001121 . } dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_provenance { dgn-np:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_assertion dcterms:description "[The 1173T and -1639A allele variants in VKORC1 gene, associated with warfarin sensitivity, were present, as expected, mostly in low dose patients while 3730A allele, linked to warfarin resistance, has been found only in high dose patients.]. 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:23726967; 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:NP1082517.RAmj4Ea0wKAhxxQ6KIq0cVR-SAOAjBoKEHlWw_wux4Qnc130_publicationInfo { this: dcterms:created "2016-05-13T12:49:56+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" . }