Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion> ?p ?o ?g. }
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- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion type Assertion NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_head.
- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion description "[We show that de novo CHD2 and SYNGAP1 mutations are new causes of epileptic encephalopathies, accounting for 1.2% and 1% of cases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_provenance.
- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion evidence source_evidence_literature NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_provenance.
- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion SIO_000772 23708187 NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_provenance.
- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion wasDerivedFrom befree-20140225 NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_provenance.
- NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_assertion wasGeneratedBy ECO_0000203 NP870144.RA3yiSo4LA8eiWKjWLub7OC-y4oWAXlm5jIaHycJfSfGE130_provenance.