Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_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." NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_assertion evidence source_evidence_literature NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_assertion SIO_000772 20501759 NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_assertion wasDerivedFrom gad-20150221 NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_assertion wasGeneratedBy ECO_0000203 NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.
- gad-20150221 importedOn "2015-02-21" NP177041.RAE1mJ7LimHZdk5LL6CgW9Jvr1_aqciRMJermVZhVv5_A130_provenance.