@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:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_head { this: np:hasAssertion dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_assertion; np:hasProvenance dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_provenance; np:hasPublicationInfo dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_publicationInfo; a np:Nanopublication . dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_assertion a np:Assertion . dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_provenance a np:Provenance . dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_publicationInfo a np:PublicationInfo . } dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_assertion { miriam-gene:6285 a ncit:C16612 . lld:C0019693 a ncit:C7057 . dgn-gda:DGNca39d82da20bec8eeb85bf445e29b7d0 sio:SIO_000628 miriam-gene:6285, lld:C0019693; a sio:SIO_001121 . } dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_provenance { dgn-np:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_assertion dcterms:description "[Analysis of multiple viral clones showed nef gene deletions/insertions in 10 out of 15 SP, along with the coexistence of intact and defective nef gene lineages in the same individual over time, whereas these nefgene abnormalities were absent from HIV-1 strains from LTNP.]. 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:10716496; 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:NP277956.RAa0l5Un0Be7xMzaAoXTKhZWfIXKdgLQqDHYQWUZLdKuo130_publicationInfo { this: dcterms:created "2016-05-13T12:43:51+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" . }