Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion> ?p ?o ?g. }
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- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion type Assertion NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_head.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion description "[Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion evidence source_evidence_literature NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion SIO_000772 11090341 NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion wasDerivedFrom befree-2016 NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.
- NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_assertion wasGeneratedBy ECO_0000203 NP301121.RAbcN9XT--uvgNC9HhvOTele5xOrm8IK0YYZg5EGy_j9A130_provenance.