Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion> ?p ?o ?g. }
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- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion type Assertion NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_head.
- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion wasGeneratedBy ECO_0000203 NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_provenance.
- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion wasDerivedFrom befree-2016 NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_provenance.
- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion SIO_000772 21694734 NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_provenance.
- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion evidence source_evidence_literature NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_provenance.
- NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_assertion description "[Finally, we provide evidence that ISS in deletion 1p36 may be associated with deletion of KLHL17 and expand the epilepsy phenotype in that syndrome to include early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP904004.RAskATsLUBgNTktnm4YTzRoKZHjhLh11knjJ_aPB3d6qo130_provenance.