Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion> ?p ?o ?g. }
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- NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_assertion type Assertion NP956978.RAtg6X2kGn20efnSNLCHTmIDQLnnac0NcoDyQQyHSECz8130_head.
- 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.