Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_assertion description "[This study showed that the patient had gp91-phox deficient CGD while his older brother was a CGD carrier and a Klinefelter, who had inherited both his mother's X chromosomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_assertion evidence source_evidence_literature NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_assertion SIO_000772 23859418 NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_assertion wasDerivedFrom befree-2016 NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_assertion wasGeneratedBy ECO_0000203 NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1094238.RAHOF32KX56G_C7CK4Bm3OsnExVQmK2nDLJk1MRKhaUAo130_provenance.