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- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion type Assertion NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_head.
- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion wasGeneratedBy ECO_0000203 NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_provenance.
- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion wasDerivedFrom befree-20150227 NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_provenance.
- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion SIO_000772 11840194 NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_provenance.
- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion evidence source_evidence_literature NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_provenance.
- NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_assertion description "[Its position in a region of linkage for autosomal dominant orthostatic hypotensive disorder and its potential role in regulating ENaC make NEDD4L a candidate gene for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870906.RABQgKBvy9hkofTh0w48KB_-n_09LI50aXLE8mjDqN4oY130_provenance.