Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_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." NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_assertion evidence source_evidence_literature NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_assertion SIO_000772 11290809 NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_assertion wasDerivedFrom befree-2016 NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_assertion wasGeneratedBy ECO_0000203 NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.
- befree-2016 importedOn "2016-02-19" NP313557.RA31Z3aL5eQ_bA7k4nFsn1I1cl-A9N0Wog2454AHoIBXk130_provenance.