Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion> ?p ?o ?g. }
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- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion type Assertion NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_head.
- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion description "[Based on the presence of additional hand anomalies, we have previously distinguished DBQD type 1 and identified CANT1 (calcium activated nucleotidase 1) mutations as responsible for DBQD type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_provenance.
- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion evidence source_evidence_literature NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_provenance.
- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion SIO_000772 24581741 NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_provenance.
- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion wasDerivedFrom befree-20150227 NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_provenance.
- NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_assertion wasGeneratedBy ECO_0000203 NP968280.RA-eoGNjJ-zS0NCXaweeBaBG-QHvcavQUTexIdC8n74OA130_provenance.