Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_assertion description "[In accord, loss of function mutations in ENaC (PHA1) cause hypotension, whereas gain of function mutations (Liddle syndrome) result in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_assertion evidence source_evidence_literature NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_assertion SIO_000772 18691017 NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_assertion wasDerivedFrom befree-20150227 NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_assertion wasGeneratedBy ECO_0000203 NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683630.RAF8WdGXfh_rMK0p6ThOz40Gm0PQKozcNU2vuV548b9_g130_provenance.