Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_assertion description "[This paper provides a concise review of the 24 published studies that evaluated the risk of SCCHN in relation to two deletion polymorphisms of the glutathione S-transferase family: GSTM1 and GSTT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_assertion evidence source_evidence_literature NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_assertion SIO_000772 11447041 NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_assertion wasDerivedFrom befree-20140225 NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_assertion wasGeneratedBy ECO_0000203 NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP876379.RAzWH5WEouyueCOH0e9QzxUntjGM87abZw8v1zW8vMdMA130_provenance.