Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_assertion description "[In 42 patients with primary CNS lymphoma (PCNSL) treated with a systemic and intraventricular high-dose MTX-based polychemotherapy, the presence of a risk haplotype defined by polymorphisms influencing methionine metabolism referred a relative risk for CNS white matter changes of 4.7 (p = 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_assertion evidence source_evidence_literature NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_assertion SIO_000772 15753437 NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_assertion wasDerivedFrom befree-20140225 NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_assertion wasGeneratedBy ECO_0000203 NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP402388.RA2TmUNVdZmtmwqrZfQqP8eiDT-WSHPDWBEjHNwiGeFyw130_provenance.