Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion description "[Acute intermittent porphyria (AIP) is an autosomal dominant inherited disease caused by a decreased activity of hydroxymethylbilane synthase (HMBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion evidence source_evidence_literature NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion SIO_000772 10944860 NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion wasDerivedFrom befree-20150227 NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_assertion wasGeneratedBy ECO_0000203 NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP459170.RAVvX4bgr-stODe-zqMb1q_kDiTGAiQKmyvd0LjbPsDBg130_provenance.