{"@type": "dcat:Dataset", "accessLevel": "public", "bureauCode": ["009:25"], "contactPoint": {"@type": "vcard:Contact", "fn": "NIH/NCBI Data Team", "hasEmail": "mailto:info@ncbi.nlm.nih.gov"}, "description": "A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.", "distribution": [{"@type": "dcat:Distribution", "description": "Access the complete Patent AT-E399860-T1: [Translated] MUTATION WITHIN THE CONNEXIN 26 GENE AND RELATION TO PRELINGUAL SYNDROMELESS DEAFNESS AND DETECTION METHODS on the official website.", "downloadURL": "https://pubchem.ncbi.nlm.nih.gov/patent/AT-E399860-T1", "mediaType": "text/html", "title": "Official Data Source"}], "identifier": "https://healthdata.gov/api/views/6qwr-me8n", "issued": "2025-09-05", "keyword": ["chemistry", "innovation", "patent", "pubchem", "research"], "landingPage": "https://healthdata.gov/d/6qwr-me8n", "modified": "2025-09-06", "programCode": ["009:066"], "publisher": {"@type": "org:Organization", "name": "National Center for Biotechnology Information (NCBI)"}, "theme": ["NIH"], "title": "Patent AT-E399860-T1: [Translated] MUTATION WITHIN THE CONNEXIN 26 GENE AND RELATION TO PRELINGUAL SYNDROMELESS DEAFNESS AND DETECTION METHODS"}