http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#head http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#assertion http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#provenance http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#assertion http://rdf.disgenet.org/resource/gda/DGN8267b64b12fb01fd9c53f921bff96195 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4360 http://rdf.disgenet.org/resource/gda/DGN8267b64b12fb01fd9c53f921bff96195 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C1333990 http://rdf.disgenet.org/resource/gda/DGN8267b64b12fb01fd9c53f921bff96195 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#provenance http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#assertion http://purl.org/dc/terms/description [In many individuals suspected of the common cancer predisposition Lynch syndrome, variants of unclear significance (VUS), rather than an obviously pathogenic mutations, are identified in one of the DNA mismatch repair (MMR) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#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/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/23690608 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#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/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/dc/terms/created 2017-10-17T13:14:42+02:00 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP708100.RAaa_X5rOU7Z6E6M5SHd78_3zE2tXBW2us4I2eq43KOZc 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