Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_assertion wasGeneratedBy ECO_0000203 NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_assertion wasDerivedFrom befree-2016 NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_assertion SIO_000772 11260246 NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_assertion evidence source_evidence_literature NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.
- NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_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." NP311681.RA0gO4lV-_-1EeYf2Ly34iDZ5RA2p7KEgo5wer34wDnLc130_provenance.