Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_assertion description "[We report on a patient with a contiguous interstitial germline deletion of chromosome 10q23, encompassing BMPR1A and PTEN, with clinical manifestations of juvenile polyposis and minor symptoms of Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_assertion evidence source_evidence_literature NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_assertion SIO_000772 22993021 NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_assertion wasDerivedFrom befree-2016 NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_assertion wasGeneratedBy ECO_0000203 NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1014334.RA5WTteV0dreHTTqiTx2khFsP6ZaJd8vcjrJXmzhqzsWQ130_provenance.