@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:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_head { this: np:hasAssertion dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_assertion; np:hasProvenance dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_provenance; np:hasPublicationInfo dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_publicationInfo; a np:Nanopublication . dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_assertion a np:Assertion . dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_provenance a np:Provenance . dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_publicationInfo a np:PublicationInfo . } dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_assertion { miriam-gene:100507436 a ncit:C16612 . lld:C0025202 a ncit:C7057 . dgn-gda:DGNfc79b98824c9f578c0c3d09b7ece1255 sio:SIO_000628 miriam-gene:100507436, lld:C0025202; a sio:SIO_001121 . } dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_provenance { dgn-np:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_assertion dcterms:description "[In conclusion, the results of the present study (i) demonstrate that the frequency of HLA class I allospecificity abnormalities in primary melanoma lesions is markedly higher than that of total HLA class I antigen downregulation described in the literature; (ii) corroborate our previous findings that staining of melanoma lesions with mAb to monomorphic determinants of HLA class I antigens does not detect selective HLA class I allospecificity loss; and (iii) demonstrate for the first time selective loss of antigenic determinants expressed on HLA class I molecules in melanoma lesions.]. 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:15853896; 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:NP280440.RAPA--iX5AXS49Zs0Ur1Q_FMroVWfqXDy3K6apy25NOeE130_publicationInfo { this: dcterms:created "2014-10-02T12:34:38+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" . }