Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_assertion description "[It was the aim of this study to determine the associations of clinical and laboratory data with plasma homocyst(e)ine levels in patients with transient ischemic attack (TIA) or minor stroke (MS), with special reference to their 677C to T mutation status in the 5,10-methylenetetrahydrofolate reductase (5,10-MTHFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_assertion evidence source_evidence_literature NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_assertion SIO_000772 9562260 NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_assertion wasDerivedFrom befree-20140225 NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_assertion wasGeneratedBy ECO_0000203 NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP829996.RAPKglXw0fkdYaRO7xyOodJmCR4AcxSlJK-i_6tnaQ1q0130_provenance.