Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion> ?p ?o ?g. }
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- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion type Assertion NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_head.
- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion description "[Within nine dentin dysplasia (DD) (type II) and dentinogenesis imperfecta (type II and III) patient/families, seven have 1 of 4 net -1 deletions within the approximately 2-kb coding repeat domain of the DSPP gene while the remaining two patients have splice-site mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_provenance.
- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion evidence source_evidence_literature NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_provenance.
- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion SIO_000772 18521831 NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_provenance.
- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion wasDerivedFrom befree-2016 NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_provenance.
- NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_assertion wasGeneratedBy ECO_0000203 NP674767.RADVr1Ko8E592faBnIfv2sR8wzwIJ77T8CA8Gmd7kDND4130_provenance.