Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion description "[Primary pigmented nodular adrenocortical disease (PPNAD) and pituitary adenoma in a boy with sporadic Carney complex due to a novel, de novo paternal PRKAR1A mutation (R96X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion evidence source_evidence_literature NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion SIO_000772 17396442 NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion wasDerivedFrom befree-20150227 NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_assertion wasGeneratedBy ECO_0000203 NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP642260.RAc1GHNQeU6U5T7KBEZiAfsdv3XZR-RoqnD08dVnMasNw130_provenance.