Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion> ?p ?o ?g. }
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- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion type Assertion NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_head.
- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_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." NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion evidence source_evidence_curated NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion SIO_000772 11090341 NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion wasDerivedFrom uniprot-20130724 NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_assertion wasGeneratedBy ECO_0000218 NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.