@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs
> .
@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:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_head
{
this:
np:hasAssertion
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_assertion
;
np:hasProvenance
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_assertion
a
np:Assertion
.
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_provenance
a
np:Provenance
.
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_assertion
{
miriam-gene:100130958
a
ncit:C16612
.
lld:C0268307
a
ncit:C7057
.
dgn-gda:DGN94fa36fdc9fc09833230c05eefb31ba5
sio:SIO_000628
miriam-gene:100130958
,
lld:C0268307
;
a
sio:SIO_001121
.
}
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_provenance
{
dgn-np:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_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:NP198651.RAXzfgOtvmaU4geQvSxWZp_LcM5PFVAWuoTU48oFonBZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:49+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" .
}