Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_assertion description "[A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), and p40(phox) of the leukocyte nicotinamide dinucleotide phosphate reduced (NADPH) oxidase leads to autosomal recessive (AR) CGD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_assertion evidence source_evidence_literature NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_assertion SIO_000772 23910690 NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_assertion wasDerivedFrom befree-20140225 NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_assertion wasGeneratedBy ECO_0000203 NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP783448.RAnoW8JbOESUGXYWD_XKJQ2R0pVN8UurMTJczcxF4unAY130_provenance.