Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion type Assertion NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_head.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_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." NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_provenance.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion evidence source_evidence_literature NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_provenance.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion SIO_000772 21997392 NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_provenance.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion wasDerivedFrom befree-2016 NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_provenance.
- NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_assertion wasGeneratedBy ECO_0000203 NP930938.RAEapOepHN1wra4oRoIfNqBHawMOAzSkL_-q3haXWSutM130_provenance.