@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:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_head { this: np:hasAssertion dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_assertion; np:hasProvenance dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_provenance; np:hasPublicationInfo dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_publicationInfo; a np:Nanopublication . dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_assertion a np:Assertion . dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_provenance a np:Provenance . dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_publicationInfo a np:PublicationInfo . } dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_assertion { miriam-gene:7262 a ncit:C16612 . lld:C0006826 a ncit:C7057 . dgn-gda:DGN5a067b161dfba208c83886ebb9e9f148 sio:SIO_000628 miriam-gene:7262, lld:C0006826; a sio:SIO_001121 . } dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_provenance { dgn-np:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_assertion dcterms:description "[Our laboratory has found genomic imprinting of a large genomic domain of human 11p15.5, identifying six imprinted genes within this domain: (a) insulin-like growth factor II (IGF-II), an important autocrine growth factor in a wide variety of malignancies; (b) H19, an untranslated RNA that is a putative growth suppressor gene regulating IGF-II; (c) p57KIP2, a cyclin-dependent kinase inhibitor that causes G1-S arrest; (d) KvLQT1, a voltage-gated potassium channel; (e) TSSC3, a gene that is homologous to mouse TDAG51, which is implicated in Fas-mediated apoptosis; and (f) TSSC5, a putative transmembrane protein-encoding gene.]. 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:10197590; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP378426.RA2QMmfzfnPLJUAJ0Ytr7BN0-PM-oIIsXWs4KpNhQnI_A130_publicationInfo { this: dcterms:created "2014-10-02T12:35:41+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }