Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion description "[Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion evidence source_evidence_literature NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion SIO_000772 7706766 NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion wasDerivedFrom befree-2016 NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_assertion wasGeneratedBy ECO_0000203 NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1319171.RAjqbLOF8am9mfO_GNZ58I3545-AaxYU-k4Mz8fKIMeR4130_provenance.