Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion> ?p ?o ?g. }
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- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion type Assertion NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_head.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion description "[PEX1 is the causative gene for PBDs of complementation group E (CG-E, CG1 in the U.S.A. and Europe), the PBDs of highest incidence, encoding the peroxin Pex1p of the AAA ATPase family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion evidence source_evidence_literature NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion SIO_000772 11439091 NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion wasDerivedFrom befree-20150227 NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.
- NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_assertion wasGeneratedBy ECO_0000203 NP1014420.RAwHqsvA0XnHUTXjoVxhTlwycP6akZPc-wAJ3Wd4Ypc80130_provenance.