Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion> ?p ?o ?g. }
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- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion type Assertion NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_head.
- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_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." NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_provenance.
- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion evidence source_evidence_literature NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_provenance.
- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion SIO_000772 23708187 NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_provenance.
- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion wasDerivedFrom befree-2016 NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_provenance.
- NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_assertion wasGeneratedBy ECO_0000203 NP1080724.RAb1Z0YKgBarwN7y_ZqDurMV-oz8pokTsRYE7-kjLpgco130_provenance.