Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_assertion description "[The aim of the study is to investigate the relevance of rs1056663 and rs2708861 HUS1 polymorphisms, and rs104548, rs2981582 and rs2910164 polymorphisms of CASP8, FGFR2 and micro RNA 146A genes, respectively, as risk modifiers in hereditary breast or ovarian cancer (BC/OC) and risk factors in sporadic BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_assertion evidence source_evidence_literature NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_assertion SIO_000772 22926736 NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_assertion wasDerivedFrom befree-2016 NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_assertion wasGeneratedBy ECO_0000203 NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1008432.RAQfzQM8ukpZHKVp9nrpD5DO9JdHKPZuMEswZN5mJDkHE130_provenance.