Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_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." NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_assertion evidence source_evidence_curated NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_assertion SIO_000772 20805988 NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_assertion wasDerivedFrom ctd_human-20130708 NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_assertion wasGeneratedBy ECO_0000218 NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP11830.RAv3W7OHv8ubP3mH7jfoNaFgvrCT3V1JdWX_LxxyVFHMI130_provenance.