Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_assertion description "[The RP genechip provides the significant advantage of detecting novel variants and could be expected to detect at least one pathogenic variant in more than 50% of patients. The APEX array provides a reliable method to detect known pathogenic variants in a]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_assertion evidence source_evidence_literature NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_assertion SIO_000772 20591486 NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_assertion wasDerivedFrom gad-20150221 NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_assertion wasGeneratedBy ECO_0000203 NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.
- gad-20150221 importedOn "2015-02-21" NP143201.RAmlyoGISmOug03ywLI34-5yCGwKiO8sAU3oj8GJ9Vbig130_provenance.