Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- befree-20150227 importedOn "2015-02-27" NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_assertion wasGeneratedBy ECO_0000203 NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_assertion wasDerivedFrom befree-20150227 NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_assertion SIO_000772 19507653 NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_assertion evidence source_evidence_literature NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.
- NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_assertion description "[Examination established hereditary thrombophilia: the heterozygotic type gene for MTHFR (C677), deletion/insertion polymorphism for PAI-1 (4G/5G) in women and deletion/insertion polymorphism 4G/5G for PAI-1 and heterozygotic genotype DD (190 bp) for angiotensin converting enzyme (ACE) in man.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350473.RA85j4Eaz1dOr1inKPbcQXS8xN1SRUsDoM9uwW0ZR5L68130_provenance.