@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:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_head { this: np:hasAssertion dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_assertion; np:hasProvenance dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_provenance; np:hasPublicationInfo dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_publicationInfo; a np:Nanopublication . dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_assertion a np:Assertion . dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_provenance a np:Provenance . dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_publicationInfo a np:PublicationInfo . } dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_assertion { miriam-gene:9260 a ncit:C16612 . lld:C0024299 a ncit:C7057 . dgn-gda:DGN524499e1eb5bd4f81e3f9964606a90e3 sio:SIO_000628 miriam-gene:9260, lld:C0024299; a sio:SIO_001121 . } dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_provenance { dgn-np:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_assertion dcterms:description "[To assess the frequency and molecular polymorphism of malignancy-associated latent membrane protein 1 (LMP1) variants in human immunodeficiency virus type 1 (HIV-1) infection, 94 B-lymphoblastoid cell lines spontaneously derived from peripheral blood mononuclear cells (PBMC) and 30 PBMC samples at seroconversion and later (mean, 55 months) were analyzed by longitudinal comparative sequence analysis in 8 patients progressing to non-Hodgkin's lymphoma (AIDS-NHL), 7 patients to opportunistic infections, and 2 patients with long-term asymptomatic HIV-1 infection.]. 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:9841847; 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:NP1410323.RAeIgvnZEgkK1EycGiIKqv3VLh1TYIlF9OHvJCsg_v6Do130_publicationInfo { this: dcterms:created "2016-05-13T12:52:26+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" . }