Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_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." NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_assertion evidence source_evidence_literature NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_assertion SIO_000772 22956460 NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_assertion wasDerivedFrom befree-20150227 NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_assertion wasGeneratedBy ECO_0000203 NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP583531.RAInhP-GBJquSrDsSzrRRYK-Hc5blL2JbDVlJw1-sf88c130_provenance.