Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_assertion description "[The demonstration that Ptch1 overexpression in trisomic NPCs is due to an APP fragment provides a link between this trisomic gene and the defective neuronal production that characterizes the DS brain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_assertion evidence source_evidence_literature NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_assertion SIO_000772 21266456 NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_assertion wasDerivedFrom befree-20140225 NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_assertion wasGeneratedBy ECO_0000203 NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP191609.RAjoFH14kL68WvgzOCTMxthJ6W9ZBYXRDCjaXy5FR6tYo130_provenance.