Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion> ?p ?o ?g. }
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- NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_assertion type Assertion NP343268.RATMXBHPLzcI5abrNsV207xFBC0DIu2N-n0xUeR18vHcI130_head.
- 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.