Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_assertion description "[Large meta-analyses confirmed the association between IL8, IL10, TNF-b, TP53 and PSCA, while genetic variation at different genes such as XPG, PLCE1, HFE, ERCC5, EZH2, DOC2, CYP19A1, ALDH2, and CDH1 have been reported to be associated with GC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_assertion evidence source_evidence_literature NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_assertion SIO_000772 24011243 NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_assertion wasDerivedFrom befree-20150227 NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_assertion wasGeneratedBy ECO_0000203 NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP750689.RAp_7Iew16uf3fT-vnuCdMgKlIqpocBWKL6on21pfGrrU130_provenance.