Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion> ?p ?o ?g. }
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- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion type Assertion NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_head.
- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion description "[the first description of a mutation in cytoskeletal, or nonmuscle, actin; with an autosomal dominant, progressive, sensorineural hearing loss phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.
- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion evidence source_evidence_literature NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.
- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion SIO_000772 13680526 NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.
- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion wasDerivedFrom lhgdn-20090331 NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.
- NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_assertion wasGeneratedBy ECO_0000203 NP136191.RA9YAZSEeNKAlqAL37WGkry9LUBC-H1JJ4hIADDooJV6I130_provenance.