Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion> ?p ?o ?g. }
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- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion type Assertion NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_head.
- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion wasGeneratedBy ECO_0000203 NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_provenance.
- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion wasDerivedFrom befree-2016 NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_provenance.
- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion SIO_000772 11713099 NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_provenance.
- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion evidence source_evidence_literature NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_provenance.
- NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_assertion description "[Mutations in DNAI1 are causative for PCD with ODA defects, and are likely the genetic origin of clinical disease in some PCD patients with ultrastructural defects in the ODA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP336750.RAA0J8NWHozKRJfJVpJte2WOxX6vSWSBYKaY9w5tcYU60130_provenance.