Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion> ?p ?o ?g. }
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- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion type Assertion NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_head.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion description "[Mutations in the connexin26 (Cx26) gene are not only a major cause of nonsyndromic deafness, but can also cause syndromic forms of hearing loss that are associated with palmoplantar keratoderma (PPK, i.e., Vohwinkel's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion evidence source_evidence_literature NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion SIO_000772 10751668 NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion wasDerivedFrom befree-20140225 NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.
- NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_assertion wasGeneratedBy ECO_0000203 NP789490.RAtvClxyO_O5ADx72WgKZTDG8VXC8qe7mBYv8IQZH_nqk130_provenance.