Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion> ?p ?o ?g. }
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- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion type Assertion NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_head.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion description "[In the remaining 5 individuals with PCD who underwent exome sequencing, we identified mutations in two genes (DNAI2, DNAH5) known to cause PCD, including an Ashkenazi Jewish founder mutation in DNAI2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion evidence source_evidence_literature NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion SIO_000772 23261302 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion wasDerivedFrom befree-2016 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.
- NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_assertion wasGeneratedBy ECO_0000203 NP1038011.RA0Saj1A0OyZfuFPNqpUbzLcPgFRj3jAesdQlCVYnVbew130_provenance.