Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_assertion description "[Two recently published studies demonstrated a strong association of genetic variants in the gene that encodes the molecular motor protein nonmuscle myosin 2a (MYH9) with ESRD in African American patients without diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_assertion evidence source_evidence_literature NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_assertion SIO_000772 18923054 NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_assertion wasDerivedFrom befree-2016 NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_assertion wasGeneratedBy ECO_0000203 NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.
- befree-2016 importedOn "2016-02-19" NP698191.RAYMTyVH2UNwxTsbN2T9p2ZqzRdJAshZ5WtMkXc98TRGY130_provenance.