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- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion type Assertion NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_head.
- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion description "[Dominant negative mechanism underlies autosomal dominant Stargardt-like macular dystrophy linked to mutations in ELOVL4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_provenance.
- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion evidence source_evidence_literature NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_provenance.
- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion SIO_000772 16036915 NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_provenance.
- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion wasDerivedFrom befree-20140225 NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_provenance.
- NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_assertion wasGeneratedBy ECO_0000203 NP877948.RA1FWRJd-GHJQTNR1qiT7Xa6AKeXmS1B05vK1rPR4Yjvs130_provenance.