Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_assertion description "[The regulatory subunit type 1-alpha (RIalpha) of protein kinase A (PKA) (the PRKAR1A gene) is mutated in most patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_assertion evidence source_evidence_literature NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_assertion SIO_000772 19063937 NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_assertion wasDerivedFrom befree-2016 NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_assertion wasGeneratedBy ECO_0000203 NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP707770.RAC7DtQsi6L0COM1Of3maCjj699v62LwzMzcob2g8t1CQ130_provenance.