Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion> ?p ?o ?g. }
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- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion type Assertion NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_head.
- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion description "[The Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI) is a lysosomal storage disease with autosomal recessive inheritance caused by deficiency of the enzyme arylsulfatase B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_provenance.
- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion evidence source_evidence_literature NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_provenance.
- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion SIO_000772 1718978 NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_provenance.
- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion wasDerivedFrom befree-20140225 NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_provenance.
- NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_assertion wasGeneratedBy ECO_0000203 NP208876.RAY00EGjaMODRG9OEJ1cI8pmS3zf68IGa6RAzJ6q7iUD0130_provenance.