Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_assertion description "[Recently, exome sequencing studies have revealed that the SWI/SNF (switch/sucrose nonfermentable) members PBRM1 and ARID1A are mutated in ccRCC, and it has also been suggested that aberrant chromatin regulation is a key step in kidney cancer pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_assertion evidence source_evidence_literature NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_assertion SIO_000772 23416164 NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_assertion wasDerivedFrom befree-2016 NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_assertion wasGeneratedBy ECO_0000203 NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1053564.RAYn7dAy4lve4vwBFwEHlp4j0QV04koaElDuXholn3ezE130_provenance.