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- source_evidence_literature type ECO_0000212 NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_assertion description "[Mucopolysaccharidosis type VI (MPS VI) is an autosomal recessive lysosomal storage disease caused by a deficiency of N-acetylgalactosamine-4-sulphatase (arylsulfatase B, ASB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_assertion evidence source_evidence_literature NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_assertion SIO_000772 11802522 NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_assertion wasDerivedFrom befree-2016 NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_assertion wasGeneratedBy ECO_0000203 NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.
- befree-2016 importedOn "2016-02-19" NP342578.RAEQNoV2tehhLBacq-Z6aEoudFYYS9foeNR724_7KXuww130_provenance.