Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion> ?p ?o ?g. }
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- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion type Assertion NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_head.
- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion wasGeneratedBy ECO_0000203 NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_provenance.
- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion wasDerivedFrom befree-2016 NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_provenance.
- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion SIO_000772 23161787 NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_provenance.
- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion evidence source_evidence_literature NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_provenance.
- NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_assertion description "[rs2736100 (TERT) and rs6010620 (RTEL1) risk alleles were associated with high-grade disease, EGFR amplification, CDKN2A-p16-INK4a homozygous deletion, and 9p and 10q deletion; rs4295627 (CCDC26) and rs498872 (PHLDB1) were associated with low-grade disease, IDH mutation, and 1p-19q codeletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029415.RAkU4jne-v_cdaYqQZElk9eJjdBKYwQff11kd-eRipCKY130_provenance.