http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#head http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#provenance http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://rdf.disgenet.org/resource/gda/DGNd9254ed88e7c6c5c80ffd75603fbf4d4 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5728 http://rdf.disgenet.org/resource/gda/DGNd9254ed88e7c6c5c80ffd75603fbf4d4 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0018553 http://rdf.disgenet.org/resource/gda/DGNd9254ed88e7c6c5c80ffd75603fbf4d4 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#provenance http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://purl.org/dc/terms/description [Germline mutations in PTEN have been found in the majority of cases of sporadic and familial Cowden syndrome (CS), an autosomal dominant inherited cancer syndrome characterised by multiple hamartomas and benign and malignant disease of the thyroid and breast.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/10548886 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/dc/terms/created 2017-10-17T13:15:44+02:00 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP872533.RAOujILKbchZ6rtlECKt4iGDWJG866kUXvW5ZIB1GWvZk http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0