Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_assertion description "[Mutations in the fatty acid 2-hydroxylase gene are associated with leukodystrophy with spastic paraparesis and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_assertion evidence source_evidence_literature NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_assertion SIO_000772 19068277 NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_assertion wasDerivedFrom befree-20150227 NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_assertion wasGeneratedBy ECO_0000203 NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP942818.RAxE2hGK2dkbGfkE4WoUOVLKluCsBvzu4Y-_Km56vbBpc130_provenance.