Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_assertion description "[MYH9 is a podocyte-expressed gene encoding nonmuscle myosin IIA that is associated with idiopathic and human immunodeficiency virus-associated focal segmental glomerulosclerosis (FSGS) and hypertensive end-stage renal disease in African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_assertion evidence source_evidence_literature NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_assertion SIO_000772 19153477 NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_assertion wasDerivedFrom befree-20150227 NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_assertion wasGeneratedBy ECO_0000203 NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583695.RALNhOFLXpfUQoskw-EcJ4W9XCbYb1riqZVtWxTVO2nYg130_provenance.