Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_assertion description "[Therefore, on one hand our data confirm a role of driver mutations for copy number alterations (CNAs) included in the GBM genomic-signature (gain of chromosome 7- EGFR gene, loss of chromosome 13- RB1 gene, loss of chromosome 10-PTEN gene); on the other, it is not obvious that the new identified CNAs are passenger mutations, as they may be necessary for tumor progression specific for the individual patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_assertion evidence source_evidence_literature NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_assertion SIO_000772 23468990 NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_assertion wasDerivedFrom befree-2016 NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_assertion wasGeneratedBy ECO_0000203 NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1058647.RAej8EYtu2zd7ISkQK3NUgbq1lYywxv8c-b9xeUWFQJ3k130_provenance.