Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_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." NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_assertion evidence source_evidence_literature NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_assertion SIO_000772 15530459 NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_assertion wasDerivedFrom befree-2016 NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_assertion wasGeneratedBy ECO_0000203 NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.
- befree-2016 importedOn "2016-02-19" NP467739.RA7Af4UpvVZbqTK2ZmDEImY_Ke0-P1npi4fyeSCvegp1c130_provenance.