Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion type Assertion NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_head.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion description "[Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_provenance.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion evidence source_evidence_literature NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_provenance.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion SIO_000772 20384727 NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_provenance.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion wasDerivedFrom befree-20140225 NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_provenance.
- NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_assertion wasGeneratedBy ECO_0000203 NP490328.RA3GuA2IEuZ7DhuJ0n-vHM9b0-IlgURNebphupv0DgOZE130_provenance.