Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_assertion description "[Fanconi anemia (FA) patients have an increased risk of acute GVHD (aGVHD) after hematopoietic SCT, with hypersensitivity to DNA-cross-linking agents and defective DNA repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_assertion evidence source_evidence_literature NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_assertion SIO_000772 23222379 NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_assertion wasDerivedFrom befree-20140225 NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_assertion wasGeneratedBy ECO_0000203 NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP209638.RAD5YASCoSG_eqQMbd6JTS5WWLjktsPg7c3KqR7-p7wdU130_provenance.