Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP256925.RANYbYE7xgIfQxg9k1MfohP2HSf5gq3zJWUYR3cFwVLTs130_provenance.