Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion description "[It is highly probable that mutations of connexin genes that result in human nonsyndromic deafness cause dysfunction of cochlear gap junctions and thereby interrupt K+ ion recirculation pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion evidence source_evidence_literature NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion SIO_000772 11810458 NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion wasDerivedFrom befree-2016 NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion wasGeneratedBy ECO_0000203 NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.
- befree-2016 importedOn "2016-02-19" NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_provenance.