Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_assertion description "[The majority of GBM also have homozygous deletions of the CDKN2 (p16/MTS1) gene, resulting in cell cycle deregulation and elevated proliferation indices.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_assertion evidence source_evidence_literature NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_assertion SIO_000772 9217972 NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_assertion wasDerivedFrom befree-20140225 NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_assertion wasGeneratedBy ECO_0000203 NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP243869.RAwFiPa1N0XQHATW7O9j5Ne4Dm4PGqfDUeN44PFZcoLUY130_provenance.