Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_assertion description "[Genetic variation in GCH1 underlies important differences in endogenous BH4 availability and is a determinant of eNOS coupling, vascular redox state, and endothelial function in human vascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_assertion evidence source_evidence_literature NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_assertion SIO_000772 18598896 NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_assertion wasDerivedFrom befree-20140225 NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_assertion wasGeneratedBy ECO_0000203 NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP847358.RA7pZU0ygjnLbK71ErNyMI6mHKPvEtpQHYJYB0_nO4LK8130_provenance.