Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP473571.RAnXhn0bFwAnFb79Bz3kyr3wJlrpp21zYHOPeBSfDtO8Q130_provenance.