Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_assertion description "[Activation of Akt independent of PTEN and CTMP tumor-suppressor gene mutations in epilepsy-associated Taylor-type focal cortical dysplasias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_assertion evidence source_evidence_literature NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_assertion SIO_000772 17013611 NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_assertion wasDerivedFrom befree-20140225 NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_assertion wasGeneratedBy ECO_0000203 NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP651922.RAHfLw1xek3A0kDkPSOjflYJZfFkWYV9hOij4EtIO0ItA130_provenance.