Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_assertion description "[Moreover, no relationship between the CCR5?32 polymorphism and risk of CAD was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_assertion evidence source_evidence_literature NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_assertion SIO_000772 23312573 NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_assertion wasDerivedFrom befree-20140225 NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_assertion wasGeneratedBy ECO_0000203 NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP381995.RA4nBawjGC2lWLQJF-Kg91GAaQB1d4Rt67NPFqJS_xPPk130_provenance.