Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion description "[Human noggin (NOG) is a responsible gene for multiple synostosis syndrome (SYNS1) and proximal symphalangism (SYM1), two conditions that are recently known to be within a wider range of clinical manifestations of stapes ankylosis with symphalangism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion evidence source_evidence_literature NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion SIO_000772 22288654 NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion wasDerivedFrom befree-2016 NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion wasGeneratedBy ECO_0000203 NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.
- befree-2016 importedOn "2016-02-19" NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_provenance.