Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_assertion description "[The overall results suggest that there may be a small excess risk of HCC in individuals with GSTT1 null and possibly also with GSTM1 null genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_assertion evidence source_evidence_literature NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_assertion SIO_000772 18065725 NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_assertion wasDerivedFrom gad-20150221 NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_assertion wasGeneratedBy ECO_0000203 NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP51024.RAjNvqlJBquYOtX2Qf6bqAV3Tis31m8njdORly_q2i-nM130_provenance.