@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4
> .
@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:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_head
{
this:
np:hasAssertion
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_assertion
;
np:hasProvenance
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_provenance
;
np:hasPublicationInfo
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_assertion
a
np:Assertion
.
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_provenance
a
np:Provenance
.
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_assertion
{
miriam-gene:5244
a
ncit:C16612
.
lld:C0008370
a
ncit:C7057
.
dgn-gda:DGN40fc3c98dc40f45e10112ba719c82ebe
sio:SIO_000628
miriam-gene:5244
,
lld:C0008370
;
a
sio:SIO_001121
.
}
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_provenance
{
dgn-np:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_assertion
dcterms:description
"[Because phospholipids are a carrier and a solvent of cholesterol in hepatic bile, we hypothesized that a defect in the MDR3 gene could be the genetic basis for peculiar forms of cholesterol gallstone disease, in particular those associated with symptoms and cholestasis without evident common bile duct stone.]. 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:11313316
;
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:NP167417.RA28_V9W8AJvHoh28jFFZ1t0PqvX_0-3RBj9J9SDwJVE4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}