Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion> ?p ?o ?g. }
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- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion type Assertion NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_head.
- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion description "[Metachromatic leukodystrophy (MLD) is an inherited demyelinating disorder caused by the deficiency of arylsulphatase A (ASA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_provenance.
- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion evidence source_evidence_curated NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_provenance.
- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion SIO_000772 15326627 NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_provenance.
- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion wasDerivedFrom uniprot-20130724 NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_provenance.
- NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_assertion wasGeneratedBy ECO_0000218 NP496.RAnvWT-TcqiG3uQjX1uuQagqLbUkzZpMUUlS3mtIT6j-o130_provenance.