Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_assertion description "[A novel 574G > A RUNX2 missense mutation has been found in members of a family clinically diagnosed with CCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_assertion evidence source_evidence_literature NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_assertion SIO_000772 16244783 NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_assertion wasDerivedFrom befree-2016 NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_assertion wasGeneratedBy ECO_0000203 NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.
- befree-2016 importedOn "2016-02-19" NP519197.RAHSKkkJp-yKRMSjwc8FhOhuH47uiMbHoAsvvJJaoHRrU130_provenance.