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- source_evidence_literature type ECO_0000212 NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_assertion description "[Metachromatic leukodystrophy (MLD) is a lethal neurodegenerative disease caused by a deficiency in the lysosomal arylsulfatase A (ARSA) enzyme leading to the accumulation of sulfatides in glial and neuronal cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_assertion evidence source_evidence_literature NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_assertion SIO_000772 19837699 NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_assertion wasDerivedFrom befree-2016 NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_assertion wasGeneratedBy ECO_0000203 NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.
- befree-2016 importedOn "2016-02-19" NP769928.RABHs50je6u7JbH8-EpyGEGmi9CzN49MLDLR-qLbryFwc130_provenance.