Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_assertion description "[Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_assertion evidence source_evidence_curated NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_assertion SIO_000772 23793026 NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_assertion wasDerivedFrom ctd_human-20150221 NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_assertion wasGeneratedBy ECO_0000218 NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP13483.RA0B1nvaA5QM_31sR0O4x1eQtJICAzTgUDUInJsP3n8_E130_provenance.