Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_assertion description "[A significant positive association between the XRCC3 c.722 polymorphism and HNSCC was found, with an adjusted odds ratio (OR) of 1.96 (p=0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_assertion evidence source_evidence_literature NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_assertion SIO_000772 18768166 NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_assertion wasDerivedFrom befree-20150227 NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_assertion wasGeneratedBy ECO_0000203 NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.
- befree-20150227 importedOn "2015-02-27" NP780767.RAUf13C416nrUNZgbrCO9m773ETJT7hgJEPdgFzKnQAig130_provenance.