Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_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." NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_assertion evidence source_evidence_literature NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_assertion SIO_000772 21997392 NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_assertion wasDerivedFrom befree-20140225 NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_assertion wasGeneratedBy ECO_0000203 NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876594.RAZxWFW8nXq6UkMzbl38qF0TGYzmG7AAnFeJbpEz_5ZNg130_provenance.