Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion> ?p ?o ?g. }
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- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion type Assertion NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_head.
- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion wasGeneratedBy ECO_0000203 NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_provenance.
- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion wasDerivedFrom befree-2016 NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_provenance.
- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion SIO_000772 11968094 NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_provenance.
- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion evidence source_evidence_literature NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_provenance.
- NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_assertion description "[A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP352764.RAAgnVZc5Ar8Y1MZ7qwbASc6b40dWIpiLb3R5xvi55SEU130_provenance.