Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_assertion description "[X-linked chronic granulomatous disease (X-CGD) is a primary immunodeficiency caused by mutations in the phagocyte nicotinamide dinucleotide phosphate oxidase catalytic subunit gp91(phox).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_assertion evidence source_evidence_literature NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_assertion SIO_000772 17728796 NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_assertion wasDerivedFrom befree-2016 NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_assertion wasGeneratedBy ECO_0000203 NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.
- befree-2016 importedOn "2016-02-19" NP627347.RA1iexJVnxSkAEc-IMnxCFlkwERnls7LvJa9LpyYJkPRI130_provenance.