Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_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." NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_assertion evidence source_evidence_literature NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_assertion SIO_000772 20810544 NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_assertion wasDerivedFrom befree-2016 NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_assertion wasGeneratedBy ECO_0000203 NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.
- befree-2016 importedOn "2016-02-19" NP836483.RAEM_Zu-v0gPZ09uHC5oG7EXW2BF-nNiKHnbuzr1XIelI130_provenance.