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- source_evidence_literature type ECO_0000212 NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_assertion description "[We report a patient with myelodysplastic syndrome (refractory anemia) showing the karyotype 46,XY,+1,der(1;10)(q10;p10), resulting in trisomy 1q and monosomy 10q abnormality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_assertion evidence source_evidence_literature NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_assertion SIO_000772 17213027 NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_assertion wasDerivedFrom befree-2016 NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_assertion wasGeneratedBy ECO_0000203 NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.
- befree-2016 importedOn "2016-02-19" NP587981.RAXc1BNXQTMRhKl0sYNffVAJFGuOMOVGsUFnvYwFtWm-k130_provenance.