Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_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." NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_assertion evidence source_evidence_curated NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_assertion SIO_000772 11090341 NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_assertion wasDerivedFrom uniprot-2016 NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_assertion wasGeneratedBy ECO_0000218 NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1130.RAA2DjI1VtL2VgM6DUsG24QDGTpYqpq2R_ylaT_6Z7Heg130_provenance.