Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion type Assertion NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_head.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion description "[Hepatoerythropoietic porphyria (HEP) is an inherited metabolic disorder characterized by the accumulation of porphyrins resulting from a deficiency in uroporphyrinogen decarboxylase (UROD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion evidence source_evidence_literature NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion SIO_000772 10397714 NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion wasDerivedFrom befree-2016 NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_assertion wasGeneratedBy ECO_0000203 NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.