@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:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_head { this: np:hasAssertion dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_assertion; np:hasProvenance dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_provenance; np:hasPublicationInfo dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_publicationInfo; a np:Nanopublication . dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_assertion a np:Assertion . dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_provenance a np:Provenance . dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_assertion { miriam-gene:619501 a ncit:C16612 . lld:C1458156 a ncit:C7057 . dgn-gda:DGN86bb878e9064c31a7097f7fa8d9e7ef1 sio:SIO_000628 miriam-gene:619501, lld:C1458156; a sio:SIO_001121 . } dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_provenance { dgn-np:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_assertion dcterms:description "[Our findings provide a basis for the concept that PTPN12 protein expression is frequently decreased or lost in human HCC tissues and that decreased PTPN12 expression may represent an acquired recurrence phenotype of HCC and that PTPN12 expression may act as a biomarker of prognosis for patients with HCC.]. 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:24475046; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP1004513.RAywInl9bdMtuPkxA8NZZK0jyFpYI5XMXJ6AIq7Q_Oscw130_publicationInfo { this: dcterms:created "2015-08-25T14:48:02+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" . }