Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_assertion description "[However, GSTP1 (P < 0.0001), CYP1A1 (P < 0.0033) and Pro/ProTP53 (P < 0.0035) variants appeared more frequently in Graves' disease patients than in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_assertion evidence source_evidence_literature NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_assertion SIO_000772 17980001 NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_assertion wasDerivedFrom befree-20140225 NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_assertion wasGeneratedBy ECO_0000203 NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625606.RAwCMyutZXQhbb2JiU6YKjnBYDNSJrwhWlfLpMOLs6nAk130_provenance.