Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_assertion description "[Alterations in 3p and 11q are frequent nonrandom aberrations in NB and define a new high-risk subgroup in MYCN single copy stage 1-3 and 4s disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_assertion evidence source_evidence_literature NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_assertion SIO_000772 12538451 NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_assertion wasDerivedFrom befree-2016 NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_assertion wasGeneratedBy ECO_0000203 NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.
- befree-2016 importedOn "2016-02-19" NP380866.RAZ7BOqD7Td6ROZDXnshVZbsdz9AHxQT9BSJrWCFi0VOs130_provenance.