Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_assertion description "[Polymorphic variants of base excision repair (APE1-D148E, XRCC1-R194W, XRCC1-R399Q and OGG1-S326C), nucleotide excision repair (XPC-PAT, XPA-23G>A, ERCC1-19007T>C and XPD-L751Q), recombination (XRCC3-T241M) and alkylation damage reversal (MGMT-L84F) were tested for their potential role in the development of GC by using logistic regression models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_assertion evidence source_evidence_literature NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_assertion SIO_000772 20817763 NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_assertion wasDerivedFrom befree-20150227 NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_assertion wasGeneratedBy ECO_0000203 NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP381887.RAhMYMB96otZtq1refQsUF-jasjT6gzbs1il7lmOnha8s130_provenance.