Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_assertion description "[However, in oncogene-positive cases (BRAF(V600E) and RET/PTC1), tumors with CNA/UPD were less frequent (5/15, 33%), whereas tumors with CNA/UPD were more frequent in oncogene-negative cases (7/10, 70%), suggesting that chromosomal aberrations may play a role in the development of PTC, especially in oncogene-negative tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_assertion evidence source_evidence_literature NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_assertion SIO_000772 22558328 NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_assertion wasDerivedFrom befree-2016 NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_assertion wasGeneratedBy ECO_0000203 NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP979703.RAnDsGqDmBb4XU_xi5BGhzj4vNqqGUYcXgST_nsACqxfU130_provenance.