Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_assertion description "[The presence of the 677 C to T mutation in the MTHFR gene does not appear to represent a risk factor for development of end-stage renal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_assertion evidence source_evidence_literature NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_assertion SIO_000772 9264011 NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_assertion wasDerivedFrom befree-20150227 NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_assertion wasGeneratedBy ECO_0000203 NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP576311.RAdZL9a7LRY_2ng61RNGgXk4RlnoaboXu8Bi0s7-6ph-o130_provenance.