Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_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." NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_assertion evidence source_evidence_literature NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_assertion SIO_000772 18483342 NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_assertion wasDerivedFrom befree-20140225 NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_assertion wasGeneratedBy ECO_0000203 NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP322850.RAIEeX4Ni3PuKs0ZZOfNkOfCEJd8gizrJzQWs4CV4fxYo130_provenance.