Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_assertion description "[Autosomal dominant macular degeneration associated with 208delG mutation in the FSCN2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_assertion evidence source_evidence_literature NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_assertion SIO_000772 14609921 NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_assertion wasDerivedFrom befree-20150227 NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_assertion wasGeneratedBy ECO_0000203 NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP877843.RARXlnNqziIBf7vzXSrjwDVJrNFYWosCfCr5hlXbsUmQA130_provenance.