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- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion type Assertion NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_head.
- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion wasGeneratedBy ECO_0000203 NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_provenance.
- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion wasDerivedFrom befree-20150227 NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_provenance.
- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion SIO_000772 23227268 NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_provenance.
- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion evidence source_evidence_literature NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_provenance.
- NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_assertion description "[A spontaneous novel mutation in COL1A2 (c.1171G>A; p.Gly391Ser) causing only dentin defects and a novel mutation in PAX9 (c.43T>A; p.Phe15Ile) causing hypodontia were identified and correlated with the phenotypic presentations in the family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP319231.RADjpxxVclV6__MPI8Vsqhk6LcSfT-9DjrWdJvyQ0pFCA130_provenance.