@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:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_head { this: np:hasAssertion dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_assertion; np:hasProvenance dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_provenance; np:hasPublicationInfo dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_publicationInfo; a np:Nanopublication . dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_assertion a np:Assertion . dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_provenance a np:Provenance . dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0005699 a ncit:C7057 . dgn-gda:DGN4a2b29d53b184054f689068bfa3595c7 sio:SIO_000628 miriam-gene:7157, lld:C0005699; a sio:SIO_001122 . } dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_provenance { dgn-np:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_assertion dcterms:description "[Two functional single nucleotide polymorphisms (SNPs), p53 R72P and MDM2 SNP309, are associated with alternation of p53 activity, however the association regarding CML susceptibility and BP transformation under imatinib treatment is unclear.]. 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:23818300; 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:NP1090668.RAlZ1C3xHB2vlVVpHpIbRzs6_vXoj5_uu2GuTEEmd0JwU130_publicationInfo { this: dcterms:created "2016-05-13T12:50:00+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" . }