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- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion type Assertion NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_head.
- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion description "[Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_provenance.
- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion evidence source_evidence_literature NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_provenance.
- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion SIO_000772 21940737 NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_provenance.
- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion wasDerivedFrom befree-20150227 NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_provenance.
- NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_assertion wasGeneratedBy ECO_0000203 NP936908.RAwssRbjivSSxAjAludxMwePOClTIoCJV6XGWzdS7PTQA130_provenance.