Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion> ?p ?o ?g. }
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- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion type Assertion NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_head.
- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion wasGeneratedBy ECO_0000203 NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_provenance.
- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion wasDerivedFrom befree-20150227 NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_provenance.
- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion SIO_000772 17236141 NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_provenance.
- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion evidence source_evidence_literature NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_provenance.
- NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_assertion description "[In the family with complex brachydactyly and syndactyly, we detected a deletion of 21 bp in the imperfect GCN (where N denotes A, C, G, or T) triplet-containing exon 1 of HOXD13, which results in a polyalanine contraction of seven residues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463378.RANFxX50lG3WgiLZIMnQMaRD-FpHIsucFSRTdaizrTiNQ130_provenance.