Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion> ?p ?o ?g. }
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- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion type Assertion NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_head.
- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion description "[In the course of positional cloning of the Congenital Dyserythropoietic Anemia type I (CDAI) [MIM 224120] gene on 15q15.1-15.3, we examined a family of French origin, in which the propositus suffered from asthenoteratozoospermia and nonsyndromic deafness in addition to CDAI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_provenance.
- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion evidence source_evidence_literature NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_provenance.
- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion SIO_000772 12825070 NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_provenance.
- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion wasDerivedFrom befree-20150227 NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_provenance.
- NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_assertion wasGeneratedBy ECO_0000203 NP974669.RAU100f5EXQz7Dbuiv7B1i01R9_eK1Wob3_HTmGWWLn-E130_provenance.