Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion> ?p ?o ?g. }
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- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion type Assertion NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_head.
- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_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." NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_provenance.
- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion evidence source_evidence_literature NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_provenance.
- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion SIO_000772 9727731 NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_provenance.
- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion wasDerivedFrom befree-20140225 NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_provenance.
- NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_assertion wasGeneratedBy ECO_0000203 NP317859.RAc0qOiBkJhmLAoavhcDdwkyk4SfvbHHg0RQ4pLJ5PVWA130_provenance.