Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion> ?p ?o ?g. }
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- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion type Assertion NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_head.
- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion description "[The Wiskott-Aldrich syndrome (WAS) is an X-linked primary immunodeficiency disease, arising from mutations of the WAS-protein (WASP) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion evidence source_evidence_literature NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion SIO_000772 11290809 NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion wasDerivedFrom befree-20140225 NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_assertion wasGeneratedBy ECO_0000203 NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.