Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_assertion description "[One PDE11A inactivating mutation (R307X) was found in one ACA, 22 germ-line missense variants (18.8%) were found in adrenocortical tumors, and only 11 missense variants (5.7%) were found in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_assertion evidence source_evidence_literature NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_assertion SIO_000772 18559625 NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_assertion wasDerivedFrom befree-20140225 NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_assertion wasGeneratedBy ECO_0000203 NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP781211.RAVHS_Vt9uCCn9jJjmOoPWYQaT8YlCdjCANO52Z7Rp_VY130_provenance.