Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_assertion description "[Eleven of 177 patients with MSH2 mutations (6.21%, p<0.001 compared with the Canadian population) were found to have BCa, compared with 3 of 129 patients with MLH1 mutations (2.32%, p>0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_assertion evidence source_evidence_literature NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_assertion SIO_000772 22883484 NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_assertion wasDerivedFrom befree-20140225 NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_assertion wasGeneratedBy ECO_0000203 NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651915.RAdWs00m_25gQBZgxyF5Vf_I7cCWCfHriTKLQ6hIPMCng130_provenance.