Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_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." NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_assertion evidence source_evidence_literature NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_assertion SIO_000772 17396442 NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_assertion wasDerivedFrom befree-20140225 NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_assertion wasGeneratedBy ECO_0000203 NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870284.RAmO_NeJwYa_QG-Sgd5hZ9aw5Z9H_vydc3L9yxoKJeDMs130_provenance.