Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_assertion description "[X-linked adrenoleukodystrophy (X-ALD) is a severe neurodegenerative disease caused by loss of function of the peroxisomal transporter ABCD1 (ALD), which results in accumulation of very long chain fatty acids (VLCFAs) in organs and serum, central demyelination and peripheral axonopathy and Addison's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_assertion evidence source_evidence_literature NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_assertion SIO_000772 15489218 NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_assertion wasDerivedFrom befree-20140225 NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_assertion wasGeneratedBy ECO_0000203 NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP246352.RAja5GqXLfvC40-82bMrvM7SMeeApLyR5mxv50uG2m4wQ130_provenance.