Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion> ?p ?o ?g. }
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- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion type Assertion NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_head.
- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion description "[Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe macular and optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_provenance.
- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion evidence source_evidence_curated NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_provenance.
- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion SIO_000772 22842229 NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_provenance.
- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion wasDerivedFrom ctd_human-20150221 NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_provenance.
- NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_assertion wasGeneratedBy ECO_0000218 NP23875.RA1effkih4gp-xMi_S0gHgg-D4OEImYdJnZ-t3XOL47L4130_provenance.