Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_assertion description "[The DNMT3A -448AG polymorphism is a novel functional SNP and contributes to its genetic susceptibility to GC. -448AG can be used as a stratification marker to predict an individuals susceptibility to GC, especially in the subgroups of individuals at the a]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_assertion evidence source_evidence_literature NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_assertion SIO_000772 20128888 NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_assertion wasDerivedFrom gad-20150221 NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_assertion wasGeneratedBy ECO_0000203 NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP163651.RASm2rGHXXj35a_vHAQofjVsTRFlabqGVf2dhlk6HuyJc130_provenance.