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- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion type Assertion NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_head.
- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion description "[Within 9 dentin dysplasia (type II) and dentinogenesis imperfecta (type II and III) patient/families, 7 have 1 of 4 net -1 deletions within the a 2-kb coding repeat domain of the DSPP gene while the remaining 2 patients have splice-site mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_provenance.
- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion evidence source_evidence_literature NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_provenance.
- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion SIO_000772 18521831 NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_provenance.
- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion wasDerivedFrom lhgdn-20090331 NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_provenance.
- NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_assertion wasGeneratedBy ECO_0000203 NP238472.RAmAfigiNr3oIjB57PMQngk3dpkCVNqMM2ElqsBFOYVS4130_provenance.