Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_assertion description "[The FAS and FASLG polymorphisms may serve as a susceptible marker for SCCHN patients at high SPM risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_assertion evidence source_evidence_literature NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_assertion SIO_000772 20501759 NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_assertion wasDerivedFrom befree-20140225 NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_assertion wasGeneratedBy ECO_0000203 NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP639609.RAvR5NTSugHfwuquoS1L033H2nGVu0pg2ImN_6KJKLB3I130_provenance.