Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_assertion description "[The Grey phenotype in horses, caused by a 4.6 kb duplication in intron 6 of Syntaxin 17 (STX17), is associated with a very high incidence of cutaneous melanoma, but the molecular mechanism behind the melanomagenesis remains unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_assertion evidence source_evidence_literature NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_assertion SIO_000772 25413220 NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_assertion wasDerivedFrom befree-2016 NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_assertion wasGeneratedBy ECO_0000203 NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1238964.RAhTh8lPyeOo3oQ54pekQ-d6x9SEgqx2Sl_La84H20iCg130_provenance.