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- NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_assertion type Assertion NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_head.
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- NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_assertion wasDerivedFrom befree-20140225 NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_provenance.
- NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_assertion SIO_000772 11175790 NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_provenance.
- NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_assertion evidence source_evidence_literature NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_provenance.
- NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_assertion description "[Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195679.RA_J90FAJdUlACHZd72-pnwal_uDs14slXmY0KXBN_1kU130_provenance.