Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP824631.RACbVhDi1d17TUfb6axz7QqGvNYeeAG4WrcNSZSW_bLlU130_provenance.