Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_assertion description "[Scan of 977 nonsynonymous SNPs in CLL4 trial patients for the identification of genetic variants influencing prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_assertion evidence source_evidence_curated NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_assertion SIO_000772 18006695 NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_assertion wasDerivedFrom ctd_human-20130708 NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_assertion wasGeneratedBy ECO_0000218 NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP32564.RABSVkGe32g3qvrZUwFMngDGO65nymtCPZ-BilydQn1nI130_provenance.