Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion type Assertion NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_head.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion description "[Familial Ohtahara syndrome due to a novel ARX gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_provenance.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion evidence source_evidence_literature NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_provenance.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion SIO_000772 21108397 NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_provenance.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion wasDerivedFrom befree-20150227 NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_provenance.
- NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_assertion wasGeneratedBy ECO_0000203 NP978166.RAFNKU517nLS-HwxG78mWlaLQWxOFyV_7zkEni3S5os6A130_provenance.