Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion type Assertion NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_head.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion description "[We established a cohort of patients with myoclonus dystonia syndrome and SGCE mutations to determine the extent to which psychiatric disorders form part of the disease phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion evidence source_evidence_literature NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion SIO_000772 23365103 NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion wasDerivedFrom befree-2016 NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_assertion wasGeneratedBy ECO_0000203 NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.