Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_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." NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_assertion evidence source_evidence_literature NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_assertion SIO_000772 10397714 NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_assertion wasDerivedFrom befree-20140225 NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_assertion wasGeneratedBy ECO_0000203 NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP480253.RAZJzSV3NKwOyZYCF3zjr79nr2_AFFSQVIGdz6Usm-tU8130_provenance.