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- source_evidence_literature type ECO_0000212 NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_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." NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_assertion evidence source_evidence_literature NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_assertion SIO_000772 17396442 NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_assertion wasDerivedFrom befree-2016 NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_assertion wasGeneratedBy ECO_0000203 NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP601939.RAIqAq66jpnEFeF_3k5Mf1uZlc5IJqSHPbYJ1yldUAjCQ130_provenance.