Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion> ?p ?o ?g. }
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- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion type Assertion NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_head.
- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion description "[All together, our data implicate rare alleles in LOXHD1 in the pathogenesis of FCD and highlight how different mutations in the same locus can potentially produce diverse phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_provenance.
- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion evidence source_evidence_literature NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_provenance.
- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion SIO_000772 22341973 NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_provenance.
- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion wasDerivedFrom befree-20150227 NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_provenance.
- NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_assertion wasGeneratedBy ECO_0000203 NP968524.RAN0W4XzilPV7L6iaCYG3afEiz81ENlB_Fgc5Cb2fQ1FU130_provenance.