Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion description "[Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by a deficient activity of coproporphyrinogen IX oxidase (CPX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion evidence source_evidence_literature NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion SIO_000772 7757079 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion wasDerivedFrom befree-20140225 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_assertion wasGeneratedBy ECO_0000203 NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP422814.RAikF5WJksPVbYqo-FW3y1UyJXAsK5E7_bd4coc7X9KWM130_provenance.