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- source_evidence_literature type ECO_0000212 NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_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." NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_assertion evidence source_evidence_literature NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_assertion SIO_000772 18923054 NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_assertion wasDerivedFrom befree-20150227 NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_assertion wasGeneratedBy ECO_0000203 NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857714.RAjNFgZ9ZFE63s1Vcb9He2DmzGKR3h1-nzWPDYvF5vc6U130_provenance.