Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_assertion description "[The variant allele carriers of MSH6 (G39E) polymorphism showed a higher risk for highly malignant disease (TaG3 +T1) than the non-carriers (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_assertion evidence source_evidence_literature NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_assertion SIO_000772 17438703 NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_assertion wasDerivedFrom befree-20140225 NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_assertion wasGeneratedBy ECO_0000203 NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP781089.RAX922tLKo4PsEG1Qvn4-9q7iUDSyvoPnJt29cFEqWiEQ130_provenance.