@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_head { this: np:hasAssertion dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_assertion; np:hasProvenance dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_provenance; np:hasPublicationInfo dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_publicationInfo; a np:Nanopublication . dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_assertion a np:Assertion . dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_provenance a np:Provenance . dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_publicationInfo a np:PublicationInfo . } dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_assertion { miriam-gene:686 a ncit:C16612 . lld:C0220754 a ncit:C7057 . dgn-gda:DGNbfabfc0b0f0b8b7e90bb51d42bb8a345 sio:SIO_000628 miriam-gene:686, lld:C0220754; a sio:SIO_001121 . } dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_provenance { dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_assertion dcterms:description "[Mutation analysis performed on DNA from 21 babies with low serum biotinidase activity confirmed that 3 had profound biotinidase deficiency (less than 10% of mean normal sera biotinidase activity), 10 had partial biotinidase deficiency (10 to 30% of mean normal serum activity), 1 was homozygous for partial biotinidase deficiency, 4 were heterozygous for either profound or partial deficiency, and 3 were normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:15060693; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP274407.RAZznXQLWon3Adn7c3eWYn01zLXOjHKMPk6KDTvqHwuMA130_publicationInfo { this: dcterms:created "2015-08-25T14:40:16+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }