Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion> ?p ?o ?g. }
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- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion type Assertion NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_head.
- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion description "[In patients of African ancestry, genetic variants in APOL1, which encodes apolipoprotein L1, associate with the nondiabetic kidney diseases, focal segmental glomerulosclerosis (FSGS), HIV-associated nephropathy (HIVAN), and hypertensive nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_provenance.
- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion evidence source_evidence_literature NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_provenance.
- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion SIO_000772 21997392 NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_provenance.
- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion wasDerivedFrom befree-20150227 NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_provenance.
- NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_assertion wasGeneratedBy ECO_0000203 NP797951.RA9Qb4f5KqnEUy9_IzuP6_ZFOKoYvwB-l-Znty3xe4SBM130_provenance.