Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion> ?p ?o ?g. }
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- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion type Assertion NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_head.
- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion description "[Hereditary hemochromatosis (HH) is a genetic disease associated with iron overload, in which individuals homozygous for the mutant C282Y HFE associated allele are at risk of developing liver disease, diabetes and arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_provenance.
- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion evidence source_evidence_literature NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_provenance.
- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion SIO_000772 17904763 NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_provenance.
- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion wasDerivedFrom befree-20150227 NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_provenance.
- NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_assertion wasGeneratedBy ECO_0000203 NP446887.RAVK1P0oNOpHUmc21QaIo7cdsSboH4McJztpF-OTqSU40130_provenance.