Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion> ?p ?o ?g. }
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- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion type Assertion NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_head.
- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_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." NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_provenance.
- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion evidence source_evidence_literature NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_provenance.
- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion SIO_000772 21265945 NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_provenance.
- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion wasDerivedFrom befree-20140225 NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_provenance.
- NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_assertion wasGeneratedBy ECO_0000203 NP293971.RA2TiTaNtfHtBDcTcDlcD3hoyNBLEzvnFfOQWBmlSzOCs130_provenance.