Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion> ?p ?o ?g. }
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- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion type Assertion NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_head.
- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion wasGeneratedBy ECO_0000203 NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_provenance.
- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion wasDerivedFrom befree-20150227 NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_provenance.
- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion SIO_000772 11968094 NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_provenance.
- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_assertion evidence source_evidence_literature NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_provenance.
- NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_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." NP462823.RAuJxA0-SkXsRzJtozClwcBJt_EdEFzSiHPamHNq8tX7c130_provenance.