Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion type Assertion NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_head.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion description "[Our results support the recent identification of mutations in ECEL1 as a disease gene in DA5D and expand the clinical and allelic spectrum of this condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_provenance.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion evidence source_evidence_curated NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_provenance.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion SIO_000772 23829171 NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_provenance.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion wasDerivedFrom uniprot-2016 NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_provenance.
- NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_assertion wasGeneratedBy ECO_0000218 NP7572.RAY-UxQzxVOIfWol5NPIP2lEfFjPlXv0vlX8-i5aixhxU130_provenance.