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- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion type Assertion NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_head.
- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion wasGeneratedBy ECO_0000203 NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_provenance.
- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion wasDerivedFrom befree-20150227 NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_provenance.
- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion SIO_000772 21265945 NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_provenance.
- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion evidence source_evidence_literature NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_provenance.
- NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease caused by a deficiency of arylsulfatase A. MLD is a heterogeneous disease with variable age at onset and variable clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252746.RAC7Ohi_324B0u20Tj8dp8UdE5u7XwjQx5IflxJpGt13U130_provenance.