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- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion type Assertion NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_head.
- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion wasGeneratedBy ECO_0000203 NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_provenance.
- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion wasDerivedFrom befree-20140225 NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_provenance.
- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion SIO_000772 23434763 NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_provenance.
- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion evidence source_evidence_literature NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_provenance.
- NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_assertion description "[Osteogenesis imperfecta (OI) is a heritable bone fragility disorder that is usually due to dominant mutations in COL1A1 or COL1A2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783622.RA1tyEL915uJKLHCbPdNWzhwdCUEaIWFphCbR0VYnDe_I130_provenance.