Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_assertion description "[These coexistent mutations/epigenetic inactivations in PI3K/AKT pathway may be responsible for the unusually aggressive course of ACC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_assertion evidence source_evidence_literature NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_assertion SIO_000772 17669465 NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_assertion wasDerivedFrom befree-20140225 NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_assertion wasGeneratedBy ECO_0000203 NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477234.RAz2bhP1ZnDfU9ilHStXc3dRYPhAOiVYhV0oLcfS_ETJE130_provenance.