Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.
- 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.
- uniprot-20130724 importedOn "2013-07-24" NP1005.RArFwXr3ThLECp5zMzejSEPkQpR3vvFFG5bDAori9UExY130_provenance.