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- source_evidence_literature type ECO_0000212 NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive neurodegenerative disorder due to deficiency of the enzyme arylsulfatase A that leads to progressive, diffuse demyelination.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_assertion evidence source_evidence_literature NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_assertion SIO_000772 11815881 NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_assertion wasDerivedFrom befree-20150227 NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_assertion wasGeneratedBy ECO_0000203 NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP252818.RAhuUkXSismz0M0az2m9zpzHjUthesva7GbHsawfwza0k130_provenance.