Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_assertion description "[The FRA2C common fragile site maps to the borders of MYCN amplicons in neuroblastoma and is associated with gross chromosomal rearrangements in different cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_assertion evidence source_evidence_literature NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_assertion SIO_000772 21258086 NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_assertion wasDerivedFrom befree-2016 NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_assertion wasGeneratedBy ECO_0000203 NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.
- befree-2016 importedOn "2016-02-19" NP867109.RASX5LRrWNMbTQmNl3z7Oo5eMpe1fGFVMw9E-8NMQGVx4130_provenance.