Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion wasGeneratedBy ECO_0000203 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion wasDerivedFrom befree-20150227 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion SIO_000772 11260246 NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion evidence source_evidence_literature NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.
- NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_assertion description "[Similarly, a mutation in desmoglein 3 underlies the balding mouse phenotype, although no human mutations in desmoglein 3 have been identified to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP361729.RAAtSxpj1mo-t1-DrQxnsUmswakIMDMXZ8B1XcPAMylUo130_provenance.