Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion> ?p ?o ?g. }
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- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion type Assertion NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_head.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion description "[We identified a c.1625G > T mutation in exon 12 of COCH that co-segregates with auditory dysfunction in the pedigree.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion evidence source_evidence_literature NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion SIO_000772 16261627 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion wasDerivedFrom befree-2016 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.
- NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_assertion wasGeneratedBy ECO_0000203 NP520536.RACorPeeVe4Lb4kEbxWSbmqlgqd-oZmpOh-TKVoUUKmdw130_provenance.