Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_assertion description "[Furthermore, we discuss possible explanations for the phenotypic differences between EEM and congenital hypotrichosis with juvenile macular dystrophy (HJMD), which is also caused by CDH3 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_assertion evidence source_evidence_literature NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_assertion SIO_000772 15805154 NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_assertion wasDerivedFrom befree-20140225 NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_assertion wasGeneratedBy ECO_0000203 NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP919941.RACSXaQ8B-0I6ADq5KSUh52nRdnIRVuYs9cNLLBFOKwcg130_provenance.