Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion> ?p ?o ?g. }
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- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion type Assertion NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_head.
- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion description "[Here, we identify loss-of-function mutations in CCDC114 causing PCD with laterality malformations involving complex heart defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_provenance.
- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion evidence source_evidence_literature NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_provenance.
- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion SIO_000772 23261303 NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_provenance.
- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion wasDerivedFrom befree-2016 NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_provenance.
- NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_assertion wasGeneratedBy ECO_0000203 NP1038013.RAsfZfMXJMQeHbuz-WYz3xC6xkz-PNONO3en2KyqZx_Cs130_provenance.