Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_assertion description "[The risk of GvHD furthermore increased when recipients heterozygous for HLA-C KIR ligand groups (C1/C2) were transplanted from donors completely lacking activating KIRs (HR 6.1, 95% CI 1.9-19.2, P = 0.002).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_assertion evidence source_evidence_literature NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_assertion SIO_000772 22077388 NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_assertion wasDerivedFrom befree-20140225 NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_assertion wasGeneratedBy ECO_0000203 NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP462937.RAUPX49U_3jB_l7OfnFjdJTtLj8i4uSXiF48NOx7wdAJg130_provenance.