Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion type Assertion NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_head.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_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." NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_provenance.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion evidence source_evidence_literature NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_provenance.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion SIO_000772 23468990 NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_provenance.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion wasDerivedFrom befree-2016 NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_provenance.
- NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_assertion wasGeneratedBy ECO_0000203 NP1058646.RA1C7qGIs2D-mLTr0B8UVaL55KcpZWf_y9p-3K8vv1X_I130_provenance.