Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_assertion description "[Cowden disease (CD) is a genetically heterogeneous inherited cancer syndrome that arises predominantly from germline phosphatase and tensin homologue deleted on chromosome 10 (PTEN) mutation and increased phosphoinositide 3-kinase/mammalian target of rapamycin (PI3K/mTOR) signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_assertion evidence source_evidence_literature NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_assertion SIO_000772 21361912 NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_assertion wasDerivedFrom befree-2016 NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_assertion wasGeneratedBy ECO_0000203 NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.
- befree-2016 importedOn "2016-02-19" NP876165.RAYp07zB0WF7Q1QkpGLS7kQ3EU2vJ3AE0I2YVtU6FVQrg130_provenance.