@prefix orcid: .
@prefix dc: .
@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 np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_head {
this: np:hasAssertion dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_assertion;
np:hasProvenance dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_provenance;
np:hasPublicationInfo dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_publicationInfo;
a np:Nanopublication .
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_assertion a np:Assertion .
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_provenance a np:Provenance .
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_assertion {
miriam-gene:54658 a ncit:C16612 .
lld:C0010324 a ncit:C7057 .
dgn-gda:DGNeb1483be169d25efec55b77d86f750d4 sio:SIO_000628 miriam-gene:54658, lld:C0010324;
a sio:SIO_001122 .
}
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_provenance {
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_assertion dc:description
"[Here, we report eleven mutations (including nine novel mutations) of the B-UGT1 gene in a large series of 14 unrelated CN-I children of various geographic origins: France (seven patients: A401P, Q357X, W335X, A368T, 1223insG, A291V, K426E, K437X); Portugal (two patients: G308E); Tunisia (two patients; Q357R); Turkey (one patient: S381R); italy (two siblings: S381R).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
wi:evidence dgn-void:source_evidence_curated;
sio:SIO_000772 miriam-pubmed:7989045;
prov:wasDerivedFrom dgn-void:uniprot-2016;
prov:wasGeneratedBy eco:ECO_0000218 .
dgn-void:source_evidence_curated a eco:ECO_0000205;
rdfs:comment "Gene-disease associations manually curated."@en;
rdfs:label "DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-2016 pav:importedOn "2016-01-25"^^xsd:date .
}
dgn-np:NP8675.RAuI-5miBq13Zh4vb0MFUFKP9x04fJrF4WvlVRHnWTQlE130_publicationInfo {
this: dc:created "2016-05-13T12:41:53+02:00"^^xsd:dateTime;
dc:rights ;
dc:rightsHolder dgn-void:IBIGroup;
dc:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
pav:createdBy orcid:0000-0003-0169-8159;
pav:version "v4.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}