@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs
> .
@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:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_head
{
this:
np:hasAssertion
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_assertion
;
np:hasProvenance
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_provenance
;
np:hasPublicationInfo
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_assertion
a
np:Assertion
.
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_provenance
a
np:Provenance
.
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_assertion
{
miriam-gene:8647
a
ncit:C16612
.
lld:C0268318
a
ncit:C7057
.
dgn-gda:DGN667c7f3ed69a7929f6343546b1dd9691
sio:SIO_000628
miriam-gene:8647
,
lld:C0268318
;
a
sio:SIO_001121
.
}
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_provenance
{
dgn-np:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_assertion
dcterms:description
"[The cause of ICP remains elusive, but there is evidence that mutations in the canalicular ABC transporter phospholipid flippase (MDR3) and in the bile salt export pump (BSEP) can predispose for the development of ICP.]. 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:16890614
;
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:NP353629.RAy5pD7Ww8ubVXJvfdeAP-5meLacM4J3VYo6s_9pLfihs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}