NP573847.RAe6ScQ-90AbsD VJgV3cU-ArmFZgvgABqwe tcEiJjnw
type: Nanopublication
has assertion: NP573847.RAe6ScQ-90AbsD VJgV3cU-ArmFZgvgABqwe tcEiJjnw130 assertion
has provenance: NP573847.RAe6ScQ-90AbsD VJgV3cU-ArmFZgvgABqwe tcEiJjnw130 provenance
has publication info: NP573847.RAe6ScQ-90AbsD VJgV3cU-ArmFZgvgABqwe tcEiJjnw130 publicationInfo
created: 2016-05-13T12:46:05+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

NP573847.RAe6ScQ-90AbsD VJgV3cU-ArmFZgvgABqwe tcEiJjnw130 assertion
type: Assertion
description: [The frequency of cancer-related gene methylation in SCCs was: CDH1 (95%), p16 (20%), p14 (15%), DAPK1 (15%), MGMT (15%), RB1 (5%), RASSF1 (5%), p15 (0%), PTEN (0%), PRDM2 (0%) and p53 (0%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/17034532
was generated by: ECO_0000203

befree-2016
imported on: 2016-02-19

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0