Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_assertion description "[We conclude that germline mutations in PRKAR1A, an apparent tumour-suppressor gene, are responsible for the CNC phenotype in a subset of patients with this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_assertion evidence source_evidence_literature NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_assertion SIO_000772 10973256 NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_assertion wasDerivedFrom befree-2016 NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_assertion wasGeneratedBy ECO_0000203 NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.
- befree-2016 importedOn "2016-02-19" NP294159.RAwqZ1GrvgWZE0nipmx_5wi40QtonRrpqC_Py9mwpj4XY130_provenance.