Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1048624.RAt3HJ7WLp7SeftqvQ5RzI2wVdO5xdp7f68AGT-FI67pY130_provenance.