Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion description "[Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion evidence source_evidence_literature NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion SIO_000772 18429043 NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion wasDerivedFrom befree-20150227 NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_assertion wasGeneratedBy ECO_0000203 NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936936.RAbtBvhjCJORnB30FNkCSvrtHSbY1awZJEVx4Vn1Z_zcc130_provenance.