Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_assertion description "[We have explored the application of array-CGH to the detection of such changes on a set of 20 samples consisting of patients with eye diseases associated with changes on chromosome 6p25 together with unaffected individuals, as well as two samples from tuberous sclerosis 2 (TSC2)-affected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_assertion evidence source_evidence_literature NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_assertion SIO_000772 15221791 NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_assertion wasDerivedFrom befree-20140225 NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_assertion wasGeneratedBy ECO_0000203 NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP812107.RAocmD75CvZFa7NzQ7BbnaE6Fu6Q4bRp3QrTKETForWzg130_provenance.