Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_assertion description "[Exome sequencing identifies GRIN2A as frequently mutated in melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_assertion evidence source_evidence_curated NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_assertion SIO_000772 21499247 NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_assertion wasDerivedFrom ctd_human-2016 NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_assertion wasGeneratedBy ECO_0000218 NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP29069.RAsUQyNS5qruI91QyyvXj73ltxpKY08gaFh7cQQ3i5sqM130_provenance.