Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion> ?p ?o ?g. }
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- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion type Assertion NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_head.
- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion description "[Mutations of the fibrillin gene (FBN1) are known to cause classical Marfan's syndrome, ectopia lentis and neonatal Marfan's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_provenance.
- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion evidence source_evidence_curated NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_provenance.
- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion SIO_000772 7870075 NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_provenance.
- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion wasDerivedFrom uniprot-2016 NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_provenance.
- NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_assertion wasGeneratedBy ECO_0000218 NP8565.RAtm5XbZWDuO-ZVAYCr7xw17dOugm0jGKeHfVvvQo5tGY130_provenance.