Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_assertion evidence source_evidence_literature NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_assertion SIO_000772 21265945 NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_assertion wasDerivedFrom befree-2016 NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_assertion wasGeneratedBy ECO_0000203 NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.
- befree-2016 importedOn "2016-02-19" NP867577.RAuy05bmTBb9AmN7bEEv65645KRO6Jau640iOcR91R7qk130_provenance.