Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion> ?p ?o ?g. }
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- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion type Assertion NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_head.
- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion description "[Unexpectedly, we found that deleting exons 2-4 of Dyx1c1 in mice caused a phenotype resembling primary ciliary dyskinesia (PCD), a disorder characterized by chronic airway disease, laterality defects and male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_provenance.
- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion evidence source_evidence_literature NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_provenance.
- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion SIO_000772 23872636 NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_provenance.
- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion wasDerivedFrom befree-20150227 NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_provenance.
- NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_assertion wasGeneratedBy ECO_0000203 NP977256.RAhvc6co2idsJU0JEoMNm_iX7cVZchzJIS2JQ4o1H6AD4130_provenance.