Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_assertion description "[A region of chromosome 22 which includes APOL1 and MYH9 genes was recently identified as a risk locus for non-diabetic forms of kidney disease, including idiopathic and HIV-associated focal segmental glomerular sclerosis and kidney disease clinically attributed to hypertension among African Americans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_assertion evidence source_evidence_literature NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_assertion SIO_000772 22956460 NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_assertion wasDerivedFrom befree-20150227 NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_assertion wasGeneratedBy ECO_0000203 NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP797838.RA497CXnVFlt1aIw7vHhdT5JB_3EpeCQQAjdPYZZn66bk130_provenance.