Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_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." NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_assertion evidence source_evidence_literature NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_assertion SIO_000772 18923054 NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_assertion wasDerivedFrom befree-20150227 NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_assertion wasGeneratedBy ECO_0000203 NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857713.RAaAz8yudycK417yVg4sAOs7xdMZs43EZ9Z6GISU2uLE4130_provenance.