Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion> ?p ?o ?g. }
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- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion type Assertion NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_head.
- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion description "[Dominant mutations in GJB2, the gene encoding the human gap junction protein connexin26 (Cx26), cause hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_provenance.
- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion evidence source_evidence_literature NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_provenance.
- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion SIO_000772 20096356 NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_provenance.
- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion wasDerivedFrom befree-20140225 NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_provenance.
- NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_assertion wasGeneratedBy ECO_0000203 NP159586.RAAPF5IR8Uo2anI3Qszar6NKOv60ZTDg6-56Hjpe6CK00130_provenance.