Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_assertion description "[SMARCC1, SMARCC2, and SMARCD1 are assigned to chromosomal regions that are frequently involved in somatic rearrangements in human cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_assertion evidence source_evidence_literature NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_assertion SIO_000772 9693044 NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_assertion wasDerivedFrom befree-20140225 NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_assertion wasGeneratedBy ECO_0000203 NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP768168.RA3nbQlm_A2fVIhKbg9SkFdmowcfUM5ZDJ5SrGS7jrA7o130_provenance.