Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_assertion description "[Defective connexins (GJB2 and GJB6), pendrin (SLC26A4), K(+) channels (KCNJ10, KCNQ1, KCNE1, and KCNMA1), Na(+)-2Cl(-)-K(+) cotransporter (SLC12A2), K(+)/Cl(-) cotransporters (KCC3 and KCC4), Cl(-) channels (BSND and CLCNKA + CLCNKB), and H(+)-ATPase (ATP6V1B1 and ATPV0A4) cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_assertion evidence source_evidence_literature NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_assertion SIO_000772 17670895 NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_assertion wasDerivedFrom befree-2016 NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_assertion wasGeneratedBy ECO_0000203 NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.
- befree-2016 importedOn "2016-02-19" NP622985.RAe3QESQg1MImWCgbzvQlufsClIAZUwnwAQF56xNn5RWs130_provenance.