NP366036.RAKeXsR6dyb 3qurh qXdhfz1-LfocEBcJxzKumFvCrcs
has assertion: NP366036.RAKeXsR6dyb 3qurh qXdhfz1-LfocEBcJxzKumFvCrcs130 assertion
has provenance: NP366036.RAKeXsR6dyb 3qurh qXdhfz1-LfocEBcJxzKumFvCrcs130 provenance
has publication info: NP366036.RAKeXsR6dyb 3qurh qXdhfz1-LfocEBcJxzKumFvCrcs130 publicationInfo
type: Nanopublication
created: 2016-05-13T12:44:31+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

NP366036.RAKeXsR6dyb 3qurh qXdhfz1-LfocEBcJxzKumFvCrcs130 assertion
type: Assertion
description: [To evaluate the role of MYEOV in ESC, we tested 31 ESC cell lines and 48 primary tumors for copy number levels of MYEOVand demonstrated that MYEOV was always coamplified with CCND1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/12202983
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