Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_assertion description "[The highest frequencies of INI1 mutations for kidney tumors were seen in exons 2, 6, and 7, compared with exons 5 and 9 for CNS tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_assertion evidence source_evidence_literature NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_assertion SIO_000772 12429635 NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_assertion wasDerivedFrom befree-20140225 NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_assertion wasGeneratedBy ECO_0000203 NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP472839.RAdlF1yaXu-ldCz19wdYsA-8JIBZuRV0gS0hNuravilzg130_provenance.