Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive neurodegenerative disorder due to deficiency of the enzyme arylsulfatase A that leads to progressive, diffuse demyelination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_assertion evidence source_evidence_literature NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_assertion SIO_000772 11815881 NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_assertion wasDerivedFrom befree-2016 NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_assertion wasGeneratedBy ECO_0000203 NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.
- befree-2016 importedOn "2016-02-19" NP343490.RAo4_yt1y4d5NCVixniCLJX0N4soy-IRWIdPWm_cRrra4130_provenance.