http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#head http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#assertion http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#provenance http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#assertion http://rdf.disgenet.org/resource/gda/DGN75fe57121b10891e1457811991d1328d http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2706 http://rdf.disgenet.org/resource/gda/DGN75fe57121b10891e1457811991d1328d http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0018784 http://rdf.disgenet.org/resource/gda/DGN75fe57121b10891e1457811991d1328d http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#provenance http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#assertion http://purl.org/dc/terms/description [In conclusion, this study determines the importance of connexin 26 mutations in Bulgarian children with severe to profound congenital nonsyndromic sensorineural hearing loss, the prevalence of the different mutation variants and their relationship with the ethnical background of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#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/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/22037723 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#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/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/dc/terms/created 2017-10-17T13:13:00+02:00 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP442527.RAWvT67Q9QJUUj7f5H8uj3KVF7hayzD0ZjH6UVWMl8N58 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