Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion type Assertion NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_head.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion description "[Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_provenance.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion evidence source_evidence_curated NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_provenance.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion SIO_000772 24903190 NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_provenance.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion wasDerivedFrom uniprot-2016 NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_provenance.
- NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_assertion wasGeneratedBy ECO_0000218 NP7919.RAeZXSO27Pw1JqrytkN63_hKAzcfact_axUqssAfkt_YM130_provenance.