Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_assertion description "[MYH9 risk variants appear to be associated with primary FSGS with secondary hypertension, although nephrosclerosis may develop in response to hypertension in subjects homozygous for the MYH9 E1 risk haplotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_assertion evidence source_evidence_literature NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_assertion SIO_000772 19153477 NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_assertion wasDerivedFrom befree-20150227 NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_assertion wasGeneratedBy ECO_0000203 NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583610.RAzbdeAQtw0uipPSiWIADK2uNFW-vrJ3LU9g8j3uiVbIY130_provenance.