@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:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_head { this: np:hasAssertion dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_assertion; np:hasProvenance dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_provenance; np:hasPublicationInfo dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_publicationInfo; a np:Nanopublication . dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_assertion a np:Assertion . dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_provenance a np:Provenance . dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_publicationInfo a np:PublicationInfo . } dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_assertion { miriam-gene:4292 a ncit:C16612 . lld:C0280100 a ncit:C7057 . dgn-gda:DGNf9cf518e322fd0f02a5617c595753173 sio:SIO_000628 miriam-gene:4292, lld:C0280100; a sio:SIO_001121 . } dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_provenance { dgn-np:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_assertion dcterms:description "[The significance of this methylated region of the hMLH1 promoter is uncertain, however, our results confirm that in some patients with AML extensive methylation of hMLH1, but not of hMSH2 may occur, and as is the case in solid tumors this can be associated with the presence of a defective DNA mismatch repair pathway resulting in MSI.]. 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:12529664; 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:NP558401.RAYiKGSH7V6NsVQnEEhgo6GkEDDpegfYCmCPRJmRLijyI130_publicationInfo { this: dcterms:created "2015-08-25T14:43:12+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" . }