Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion> ?p ?o ?g. }
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- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion type Assertion NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_head.
- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion description "[Here we report that compound heterozygous and homozygous NMNAT1 mutations cause severe neonatal neurodegeneration of the central retina and early-onset optic atrophy in 22 unrelated individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_provenance.
- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion evidence source_evidence_curated NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_provenance.
- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion SIO_000772 22842229 NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_provenance.
- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion wasDerivedFrom ctd_human-20130708 NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_provenance.
- NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_assertion wasGeneratedBy ECO_0000218 NP24182.RA7SXkcYbJy0QSRxFhFLxc-UVgbHn6HDpfKN_NV9yUyAg130_provenance.