Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion type Assertion NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_head.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion description "[The genetic variants associated with the risk of glioma in the EGFR gene have also been associated with specific somatic aberrations, including loss at the CDKN2A/B locus and allele specific loss of EGFR in the tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_provenance.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion evidence source_evidence_literature NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_provenance.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion SIO_000772 24184969 NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_provenance.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion wasDerivedFrom befree-2016 NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_provenance.
- NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_assertion wasGeneratedBy ECO_0000203 NP1124455.RAeMEE9lhCfu7-oXhAZ4t6r1xDN22bsITmsEWwCAlm5bY130_provenance.