Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion> ?p ?o ?g. }
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- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion type Assertion NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_head.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_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." NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion evidence source_evidence_literature NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion SIO_000772 11810458 NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion wasDerivedFrom befree-20150227 NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.
- NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_assertion wasGeneratedBy ECO_0000203 NP1012305.RANz2BDrlkCw-J-S8O8WuAqJYgFCRCTBYEpvk9uiSIjm0130_provenance.