Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_assertion description "[The use of high-throughput next-generation sequencing techniques in multiple tumor types during the last few years has identified NTRK1, 2, and 3 gene rearrangements encoding novel oncogenic fusions in 19 different tumor types to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_assertion evidence source_evidence_literature NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_assertion SIO_000772 25527197 NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_assertion wasDerivedFrom befree-2016 NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_assertion wasGeneratedBy ECO_0000203 NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1249856.RAwRsDZBqQ2gGNeE1S3CxJyFeXgQZLVNYGEX0_Q9w-G6c130_provenance.