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- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_assertion type Assertion NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_head.
- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_assertion wasGeneratedBy ECO_0000203 NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_provenance.
- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_assertion wasDerivedFrom befree-20150227 NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_provenance.
- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_assertion SIO_000772 23434763 NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_provenance.
- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_assertion evidence source_evidence_literature NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_provenance.
- NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_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." NP319356.RAfX9ZaHy9Nw2mMEUhWd7HCKl0YwlDWCgAb5d-MahJ67o130_provenance.