Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_assertion description "[The overall penetrance of CNC among PRKAR1A mutation carriers is near 98%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_assertion evidence source_evidence_literature NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_assertion SIO_000772 21115159 NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_assertion wasDerivedFrom befree-2016 NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_assertion wasGeneratedBy ECO_0000203 NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.
- befree-2016 importedOn "2016-02-19" NP855485.RANapHqUYy6E9gQa7ds9sys27n0rpZbzdMiVJg_RJV2hY130_provenance.