Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_assertion wasGeneratedBy ECO_0000203 NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_assertion wasDerivedFrom befree-20140225 NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_assertion SIO_000772 16123401 NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_assertion evidence source_evidence_literature NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_assertion description "[To overcome these limitations, arrayed primer extension (APEX) technology was used to design a genotyping microarray for early-onset, severe retinal degenerations that includes all of the >300 disease-associated variants currently described in eight genes (in addition to the six just listed, the early-onset RP genes LRAT and MERTK were added).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717573.RAsm2c1l-gOPPRy-3cpNoscnQK1K-WGXkDqeGsZ5mpYTg130_provenance.