Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion> ?p ?o ?g. }
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- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion type Assertion NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_head.
- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion description "[The mutilating keratoderma associated with sensorineural hearing loss is thought to have an etiologic basis, resting on a mutation of the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_provenance.
- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion evidence source_evidence_literature NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_provenance.
- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion SIO_000772 11174420 NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_provenance.
- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion wasDerivedFrom befree-2016 NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_provenance.
- NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_assertion wasGeneratedBy ECO_0000203 NP307057.RApmrU4nT7p3XqmRnX-ElmBw_xqKSE6lmjdX8krGm2YvE130_provenance.