@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_assertion
a
np:Assertion
.
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_provenance
a
np:Provenance
.
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_assertion
{
miriam-gene:7361
a
ncit:C16612
.
lld:C0268306
a
ncit:C7057
.
dgn-gda:DGN909e639b16de0e59358d22f3c41632ec
sio:SIO_000628
miriam-gene:7361
,
lld:C0268306
;
a
sio:SIO_001121
.
}
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_provenance
{
dgn-np:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_assertion
dcterms:description
"[In addition, characterization of the UGT1A locus and genetic studies directed at understanding the role of bilirubin glucuronidation and the biochemical basis of the clinical symptoms found in unconjugated hyperbilirubinemia have uncovered the structural gene polymorphisms associated with Crigler-Najjar's and Gilbert's syndrome.]. 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:10836148
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP741099.RAWc93euRj3V_gfl2qyK-PTyY_eLwcGRjzBuKPE5KCNDo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
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"v2.1.0" .
}