Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_assertion description "[These deletions are close to the APC and VHL genes that confer susceptibility to familial Adenomatous polyposis (OMIM #17510) and von-Hippel-Lindau syndrome (OMIM #193300), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_assertion evidence source_evidence_literature NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_assertion SIO_000772 17954272 NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_assertion wasDerivedFrom befree-20140225 NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_assertion wasGeneratedBy ECO_0000203 NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP858981.RAKL6v6R_u8WGaU-8kKq5jTkwtRXyz5d6L87m007xMfAw130_provenance.