Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_assertion description "[We found several canonical cytogenetic alterations associated with GBM and a common minimal deleted region (MDR) at 1p36.31, including CAMTA1 gene, a putative tumor suppressor gene, specific for the GSC population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_assertion evidence source_evidence_literature NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_assertion SIO_000772 23468990 NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_assertion wasDerivedFrom befree-20140225 NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_assertion wasGeneratedBy ECO_0000203 NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583208.RAt_bjh8bEj0eZomMXMf2UFTKxqgzoqwVyiAwCSzCa8do130_provenance.