Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion> ?p ?o ?g. }
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- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion type Assertion NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_head.
- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_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." NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_provenance.
- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion evidence source_evidence_curated NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_provenance.
- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion SIO_000772 23708187 NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_provenance.
- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion wasDerivedFrom ctd_human-20150221 NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_provenance.
- NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_assertion wasGeneratedBy ECO_0000218 NP29179.RAa4DlXXou2Bj6GKsw6NbdpS7K3tOeed6Nw3cO7l0t-MM130_provenance.