Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_assertion description "[PTEN Hamartoma Tumour Syndrome (PHTS) includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), and other conditions resulting from germline mutation of the PTEN tumour suppressor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_assertion evidence source_evidence_literature NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_assertion SIO_000772 21343951 NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_assertion wasDerivedFrom befree-2016 NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_assertion wasGeneratedBy ECO_0000203 NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.
- befree-2016 importedOn "2016-02-19" NP874382.RA9hFci0HroS6fu4PO0yDrr9WnHm1HUSJjVSnoAWJ8koA130_provenance.