@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:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_head { this: np:hasAssertion dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_assertion; np:hasProvenance dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_provenance; np:hasPublicationInfo dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_publicationInfo; a np:Nanopublication . dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_assertion a np:Assertion . dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_provenance a np:Provenance . dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_publicationInfo a np:PublicationInfo . } dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_assertion { miriam-gene:7172 a ncit:C16612 . lld:C0342801 a ncit:C7057 . dgn-gda:DGN830336a193a24716c9cfc2588b034fc5 sio:SIO_000628 miriam-gene:7172, lld:C0342801; a sio:SIO_001121 . } dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_provenance { dgn-np:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_assertion dcterms:description "[We conclude that TPMT kd cells are an appropriate in vitro model to investigate the significance of TPMT deficiency with thiopurine therapy and could be helpful in understanding possible clinical consequences of TPMT polymorphism.]. 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:22972540; 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:NP1012553.RARCFL4q187sAF0X97LOJEjXh0Vcv2cHm29X6htNV46Qs130_publicationInfo { this: dcterms:created "2016-05-13T12:49:25+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" . }