@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:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_head { this: np:hasAssertion dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_assertion; np:hasProvenance dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_provenance; np:hasPublicationInfo dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_publicationInfo; a np:Nanopublication . dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_assertion a np:Assertion . dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_provenance a np:Provenance . dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_assertion { miriam-gene:2592 a ncit:C16612 . lld:C0016952 a ncit:C7057 . dgn-gda:DGN97483cfb45b036bbcee10abf7eafc3a4 sio:SIO_000628 miriam-gene:2592, lld:C0016952; a sio:SIO_001122 . } dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_provenance { dgn-np:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_assertion dcterms:description "[Six out of thirteen (46%) daughters and two mothers of the remaining seven daughters (29%) were carriers for the N314D mutation of GALT associated with the Duarte variant of galactosaemia as compared to 16 out of 113 general population controls (14%) who possessed at least one N314D allele.]. 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:9238673; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1377507.RAyrnVfHYsCT_D7L28Bc_6A5x76wpuddDh-YQCyMT1ESw130_publicationInfo { this: dcterms:created "2016-05-13T12:52:10+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }