@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:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_head { this: np:hasAssertion dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_assertion; np:hasProvenance dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_provenance; np:hasPublicationInfo dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_publicationInfo; a np:Nanopublication . dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_assertion a np:Assertion . dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_provenance a np:Provenance . dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_publicationInfo a np:PublicationInfo . } dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_assertion { miriam-gene:6777 a ncit:C16612 . lld:C0004364 a ncit:C7057 . dgn-gda:DGNbeb6f001ca256ac2848579c787bc1fe8 sio:SIO_000628 miriam-gene:6777, lld:C0004364; a sio:SIO_001121 . } dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_provenance { dgn-np:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_assertion dcterms:description "[STAT3 and STAT5b mutations can be used as molecular markers for LGL leukemia diagnostics, and they present novel therapeutic targets for STAT3 and STAT5b inhibitors, which currently are in development for treatment of cancer and autoimmune disorders.]. 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:24512550; 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:NP1153774.RAl_Zj-mj5sVjzv63h4H8YxmOgfA2-Zn2n_1Bl5nEARP4130_publicationInfo { this: dcterms:created "2016-05-13T12:50:29+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" . }