Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_assertion description "[These 2 cases provide additional evidence for the existence of a form of familial porphyria cutanea tarda in which erythrocytic uroporphyrinogen decarboxylase activity is normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_assertion evidence source_evidence_literature NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_assertion SIO_000772 2767288 NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_assertion wasDerivedFrom befree-20140225 NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_assertion wasGeneratedBy ECO_0000203 NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP192592.RAH4jxsDTIlkeYgScU2aSpe455ehlLA_O-kpG1JQ9nzT0130_provenance.