Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_assertion wasGeneratedBy ECO_0000203 NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_assertion wasDerivedFrom befree-20140225 NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_assertion SIO_000772 11669217 NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_assertion evidence source_evidence_literature NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_assertion description "[When the comparison group without severe acute GVHD was expanded to include grade I as well as grade 0 patients, the risk from CD31 nonidentity increased for both codon 563/670 (OR = 12.31, P = .010) and codon 125 (OR = 11.24, P = .011).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP737857.RAOrFtjglizj4UeF1x8i28_x93wdUfQmUzdg7LRS3gw8o130_provenance.