http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#head http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#assertion http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#provenance http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#assertion http://rdf.disgenet.org/resource/gda/DGN711939220db579732513c362f0c7516e http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/5172 http://rdf.disgenet.org/resource/gda/DGN711939220db579732513c362f0c7516e http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0339789 http://rdf.disgenet.org/resource/gda/DGN711939220db579732513c362f0c7516e http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#provenance http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#assertion http://purl.org/dc/terms/description [Whilst these findings demonstrate molecular heterogeneity for PDS mutations associated with Pendred syndrome, this study would support the use of molecular analysis of the PDS gene in the assessment of families with congenital hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#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/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/9618167 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#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/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/dc/terms/created 2017-10-17T13:15:16+02:00 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP797836.RARWEQwFoFT6EA5vIEGJ6pjUtf-Z9Kf07B7gZxIZMP1aY 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