Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_assertion description "[Overall, PRKACA somatic mutations were identified in 22 of 59 unilateral adenomas (37%) from patients with overt Cushing's syndrome; these mutations were not detectable in 40 patients with subclinical hypercortisolism or in 82 patients with other adrenal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_assertion evidence source_evidence_literature NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_assertion SIO_000772 24571724 NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_assertion wasDerivedFrom befree-20150227 NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_assertion wasGeneratedBy ECO_0000203 NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.
- befree-20150227 importedOn "2015-02-27" NP642465.RAEL3ASZ8Bd9DHhDNzHgmzlPTz0D3RaQi4dSES1eOeQno130_provenance.