@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w
> .
@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:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_head
{
this:
np:hasAssertion
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_assertion
;
np:hasProvenance
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_provenance
;
np:hasPublicationInfo
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_assertion
a
np:Assertion
.
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_provenance
a
np:Provenance
.
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_assertion
{
miriam-gene:1244
a
ncit:C16612
.
lld:C0022350
a
ncit:C7057
.
dgn-gda:DGNff31e0dad5796831d0ba2c6829f70cfc
sio:SIO_000628
miriam-gene:1244
,
lld:C0022350
;
a
sio:SIO_001121
.
}
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_provenance
{
dgn-np:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_assertion
dcterms:description
"[Several mutations in the human MRP2 gene have been identified which lead to the absence of the MRP2 protein from the hepatocyte canalicular membrane and to the conjugated hyperbilirubinemia of Dubin-Johnson 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:10581368
;
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:NP220090.RA1efZ5V8iIwHr6ddh2uMsjkIlKcD247CTEdJCzjY9V2w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}