Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion> ?p ?o ?g. }
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- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion type Assertion NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_head.
- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_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." NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_provenance.
- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion evidence source_evidence_literature NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_provenance.
- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion SIO_000772 24581741 NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_provenance.
- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion wasDerivedFrom befree-2016 NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_provenance.
- NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_assertion wasGeneratedBy ECO_0000203 NP1159008.RAIG9i2r6AugmHdR7bCJSNXFeD5Ez4BLZj5mu-zhRMAWE130_provenance.