Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion> ?p ?o ?g. }
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- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion type Assertion NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_head.
- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion description "[Together these data show that variable loss of function due to alterations in the runt and PST domains of CBFA1 may give rise to clinical variability, including classic CCD, mild CCD and isolated primary dental anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_provenance.
- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion evidence source_evidence_literature NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_provenance.
- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion SIO_000772 10545612 NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_provenance.
- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion wasDerivedFrom befree-2016 NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_provenance.
- NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_assertion wasGeneratedBy ECO_0000203 NP266714.RARUFQ18T2Nw-BQhVMbfYvd-wMb1HWC9yGhINV0v-11iU130_provenance.