Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_assertion description "[A genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_assertion evidence source_evidence_curated NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_assertion SIO_000772 20805988 NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_assertion wasDerivedFrom ctd_human-20130708 NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_assertion wasGeneratedBy ECO_0000218 NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP20853.RACbm_PK8WOqHmJ49r9VsYPUNEjRN0glBZ8vcasK0V7iE130_provenance.