Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion> ?p ?o ?g. }
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- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion type Assertion NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_head.
- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_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." NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_provenance.
- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion evidence source_evidence_curated NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_provenance.
- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion SIO_000772 23708187 NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_provenance.
- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion wasDerivedFrom uniprot-2016 NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_provenance.
- NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_assertion wasGeneratedBy ECO_0000218 NP7521.RAThleFb7Yb2-Nb_EvBERUKOaYzQ_VrYOVR1HiI9VvCeY130_provenance.