Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion> ?p ?o ?g. }
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- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion type Assertion NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_head.
- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion description "[Mucopolysaccharidosis type IIIA (MPS IIIA) is an autosomal recessive disease that occurs due to a deficiency of heparan sulfate sulfamidase (SGSH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion evidence source_evidence_literature NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion SIO_000772 11829484 NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion wasDerivedFrom befree-20140225 NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_assertion wasGeneratedBy ECO_0000203 NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.