Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion> ?p ?o ?g. }
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- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion type Assertion NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_head.
- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion description "[A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_provenance.
- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion evidence source_evidence_curated NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_provenance.
- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion SIO_000772 7757079 NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_provenance.
- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion wasDerivedFrom uniprot-20130724 NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_provenance.
- NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_assertion wasGeneratedBy ECO_0000218 NP1490.RAqmxsRJg00zeHL711ml8hafYrGiaF1pnAajs38RJWjms130_provenance.