Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion type Assertion NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_head.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_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." NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_provenance.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion evidence source_evidence_literature NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_provenance.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion SIO_000772 11815881 NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_provenance.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion wasDerivedFrom befree-2016 NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_provenance.
- NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_assertion wasGeneratedBy ECO_0000203 NP343491.RATJwwHGR-WXGZYiN9B4Qg3brZ-miVIlYIGfsEqtW0Kh0130_provenance.