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- source_evidence_literature type ECO_0000212 NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_assertion description "[No allelic variant was detected for hsa-mir-17 and hsa-mir-369, and allelic and genotype frequencies for miR-146a rs2910164 single-nucleotide polymorphism (SNP) were comparable with that of 155 controls from the same population, ruling out a role for genetic variations in these three miRNAs as major determinants in cancer predisposition of BRCA1/BRCA2-negative patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_assertion evidence source_evidence_literature NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_assertion SIO_000772 20810544 NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_assertion wasDerivedFrom befree-20150227 NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_assertion wasGeneratedBy ECO_0000203 NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP995786.RA2PtR5yGrm-ppcTo0b6fA5v_3e1h4EYzwXq3Nd_5yM8A130_provenance.