Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion> ?p ?o ?g. }
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- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion type Assertion NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_head.
- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion description "[Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_provenance.
- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion evidence source_evidence_curated NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_provenance.
- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion SIO_000772 23708187 NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_provenance.
- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion wasDerivedFrom ctd_human-2016 NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_provenance.
- NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_assertion wasGeneratedBy ECO_0000218 NP33016.RAZWaqXT0-iEI5JNaclapDHHin1p1lGH89_OF80G1iS6U130_provenance.