Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion description "[Four single nucleotide polymorphisms comprising the major MYH9 E1 risk haplotype were tested for association with estimated glomerular filtration rate (eGFR) and urine albumin:creatinine ratio (ACR) in 2,903 HyperGEN participants (1,458 African Americans (AA) in 895 families and 1,445 European Americans (EA) in 859 families) to determine the role of MYH9 in subclinical nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion evidence source_evidence_literature NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion SIO_000772 19153477 NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion wasDerivedFrom befree-2016 NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_assertion wasGeneratedBy ECO_0000203 NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP715309.RAZqQL54wnntml7wa0M4eCkpz6h9jD9gDHaRFSCXVrUWU130_provenance.