Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_assertion description "[MTHFR C677T-A1298C diplotypes were associated with risk of meningioma (P = 0.002) and glioma (P = 0.02); risks were increased with genotypes associated with reduced MTHFR activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_assertion evidence source_evidence_literature NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_assertion SIO_000772 18483342 NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_assertion wasDerivedFrom gad-20150221 NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_assertion wasGeneratedBy ECO_0000203 NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP91531.RAuVF0Kxf2AuwUoafKgPYgy6gKIb7YGl53ZDmox7fqtKc130_provenance.