@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA
> .
@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#
> .
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_head
{
this:
np:hasAssertion
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_assertion
;
np:hasProvenance
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_assertion
a
np:Assertion
.
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_provenance
a
np:Provenance
.
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_assertion
{
miriam-gene:5244
a
ncit:C16612
.
lld:C0008372
a
ncit:C7057
.
dgn-gda:DGN7c71ededf24966d703e86ad5af12e840
sio:SIO_000628
miriam-gene:5244
,
lld:C0008372
;
a
sio:SIO_001121
.
}
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_provenance
{
dgn-np:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_assertion
dcterms:description
"[The aims of the present study was to study the significance of ABCB4 mutations in mainland Chinese children with chronic intrahepatic cholestasis and to correlate genetic findings with clinical features and response to ursodeoxycholic acid (UDCA) therapy.]. 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:22343912
;
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:NP584339.RAI3dN1A4hRTdCBl-8ntIAsIkpW8lUXhZwSohZ-XdrDWA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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
<
http://orcid.org/0000-0001-5999-6269
> , <
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
pav:version
"v2.1.0" .
}