Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_assertion description "[Lack of association of eNOS (G894T) and p22phox NADPH oxidase subunit (C242T) polymorphisms with systemic sclerosis in a cohort of French Caucasian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_assertion evidence source_evidence_literature NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_assertion SIO_000772 15530459 NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_assertion wasDerivedFrom befree-20150227 NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_assertion wasGeneratedBy ECO_0000203 NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP338779.RAHLeyISmIeFPyX2vCYDyfCnYzt9KSsYr0ErdCS8sA2Xg130_provenance.