Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_assertion description "[CD46 SNP genotyping was undertaken in this individual and another patient with CFH deficiency associated with chromosome 1 uniparental isodisomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_assertion evidence source_evidence_literature NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_assertion SIO_000772 23870792 NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_assertion wasDerivedFrom befree-20140225 NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_assertion wasGeneratedBy ECO_0000203 NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP476880.RAvVtLHFQDrRnys3stGz-383B2thWm-4tgjDshwSPqubI130_provenance.