Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_assertion description "[Metachromatic leukodystrophy (MLD) is a rare lysosomal sphingolipid storage disorder, caused by a deficiency of arylsulfatase A (ASA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_assertion evidence source_evidence_literature NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_assertion SIO_000772 20571983 NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_assertion wasDerivedFrom befree-2016 NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_assertion wasGeneratedBy ECO_0000203 NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.
- befree-2016 importedOn "2016-02-19" NP820842.RARbP_3s6oruVdnTzJ1fJZHA3YvrjROq_oHmhsdC1ZW34130_provenance.