Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion> ?p ?o ?g. }
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- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion type Assertion NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_head.
- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion wasGeneratedBy ECO_0000203 NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_provenance.
- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion wasDerivedFrom befree-20140225 NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_provenance.
- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion SIO_000772 15370538 NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_provenance.
- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion evidence source_evidence_literature NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_provenance.
- NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_assertion description "[Leber congenital amaurosis (LCA; estimated prevalence 1 : 50,000-100,000) is an early-onset inherited cause of childhood blindness characterized by a severe retinal dystrophy immediately after birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP695808.RAcojjLMTfkGtWtrOb1u8vHAmLyd_PNd7VwPJCijsNNx8130_provenance.