Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_assertion description "[These aberrations were probably secondary to the primary t(12;16), and are cytogenetic evidence of clonal evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_assertion evidence source_evidence_literature NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_assertion SIO_000772 2193480 NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_assertion wasDerivedFrom befree-20140225 NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_assertion wasGeneratedBy ECO_0000203 NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.
- befree-20140225 importedOn "2014-02-25" NP837751.RA4RNimkncj6x3KVZEmfW8hlsJ3BQxUHCPiEhOWDpOt3o130_provenance.