@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:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_head { this: np:hasAssertion dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_assertion; np:hasProvenance dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_provenance; np:hasPublicationInfo dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_publicationInfo; a np:Nanopublication . dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_assertion a np:Assertion . dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_provenance a np:Provenance . dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_publicationInfo a np:PublicationInfo . } dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_assertion { miriam-gene:5728 a ncit:C16612 . lld:C1368354 a ncit:C7057 . dgn-gda:DGNf054b4e0a0405399de268f9b42fe83eb sio:SIO_000628 miriam-gene:5728, lld:C1368354; a sio:SIO_001121 . } dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_provenance { dgn-np:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_assertion dcterms:description "[Among the five HNPCC or MSI+ sporadic CRCs carrying frameshift somatic mutations with immunohistochemistry data, three had lost all PTEN expression, one showed weak PTEN expression levels, and one had mixed tumor cell populations with weak and moderate expression levels.]. 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:12163369; 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:NP655002.RAXTRPPq2t_ERaxCzuLE3qkAFtlNMIJ2H_l4QTKy8XMG0130_publicationInfo { this: dcterms:created "2015-08-25T14:44:13+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" . }