Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_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." NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_assertion evidence source_evidence_curated NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_assertion SIO_000772 21499247 NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_assertion wasDerivedFrom ctd_human-20130708 NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_assertion wasGeneratedBy ECO_0000218 NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP27958.RAqEU26vSTJxk0BwLBSu_vn5EosxZP7PEKNqg5yU4wMhw130_provenance.