Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_assertion description "[Adrenomyeloneuropathy (AMN) represents a milder form of X-linked adrenoleukodystrophy (ALD), the most frequent peroxisomal disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_assertion evidence source_evidence_literature NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_assertion SIO_000772 10480364 NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_assertion wasDerivedFrom befree-20140225 NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_assertion wasGeneratedBy ECO_0000203 NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP833840.RAp3zirTkX81wno-IuzS4xu15WHHSYV5ToFNk2jUCEhRk130_provenance.