Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive storage disease caused by deficiency of the lysosomal enzyme, arylsulfatase A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_assertion evidence source_evidence_literature NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_assertion SIO_000772 9600244 NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_assertion wasDerivedFrom befree-2016 NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_assertion wasGeneratedBy ECO_0000203 NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395848.RAbsX8rE4aDE4o56mCUXIQr-56ofjy2moRJO4Yv6eSbgM130_provenance.