Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion> ?p ?o ?g. }
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- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion type Assertion NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_head.
- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion wasGeneratedBy ECO_0000203 NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_provenance.
- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion wasDerivedFrom befree-20150227 NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_provenance.
- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion SIO_000772 11020419 NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_provenance.
- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion evidence source_evidence_literature NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_provenance.
- NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_assertion description "[Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674454.RALtEtlIh4MZ8EDW5qlczL-OQSpxmqlKjq79lwnK2efbY130_provenance.