Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_assertion description "[Hereditary hemochromatosis (HH) is a common autosomal recessive disorder that can result in iron overload and a wide range of clinical complications, including hepatic cirrhosis, diabetes mellitus, hypopituitarism, hypogonadism, arthritis, and cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_assertion evidence source_evidence_literature NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_assertion SIO_000772 9727731 NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_assertion wasDerivedFrom befree-20140225 NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_assertion wasGeneratedBy ECO_0000203 NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP595281.RA3ABG-0Z03wzyTeyYUaEWARZrE387Z4JY2-LTVCl1kwg130_provenance.