Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion description "[In conclusion, our results reveal a great diversity for KIR genotypes in donors and recipients of BMT and that the risk of GVHD was maximum in unrelated BMT when the recipient KIR genotype was included in the donor KIR genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion evidence source_evidence_literature NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion SIO_000772 12039408 NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion wasDerivedFrom gad-20150221 NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_assertion wasGeneratedBy ECO_0000203 NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP74495.RA1rvWuwguA1_vRA2nHIlMygkVa69TMlWeUBUB4MnO8Yg130_provenance.