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- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion type Assertion NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_head.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion wasGeneratedBy ECO_0000203 NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion wasDerivedFrom befree-20150227 NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion SIO_000772 23456818 NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion evidence source_evidence_literature NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.
- NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_assertion description "[Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP944909.RAYf4BexjqC_6SQTF9pl6rlJhU4F5ShDmcuH-1aGKVU4k130_provenance.