Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_assertion description "[To evaluate the role of miRNA allelic variants in the susceptibility to familial breast and ovarian cancers in BRCA1/BRCA2-negative patients, we focused our attention on three miRNAs, miR-146a, miR-17 and miR-369, based on their affinity to either BRCA1 or BRCA2 messenger RNA and their localization on chromosome regions commonly deleted in those tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_assertion evidence source_evidence_literature NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_assertion SIO_000772 20810544 NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_assertion wasDerivedFrom befree-20150227 NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_assertion wasGeneratedBy ECO_0000203 NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1001652.RAo1ahvVBx2et0dBOvFyI_3FQJR8i4o2bO5UST8HXeKrg130_provenance.