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http://rdf.disgenet.org/nanopublications.trig#NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_assertion
a
np:Assertion
.
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_provenance
a
np:Provenance
.
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_publicationInfo
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np:PublicationInfo
.
}
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_assertion
{
miriam-gene:64240
a
ncit:C16612
.
lld:C0947622
a
ncit:C7057
.
dgn-gda:DGNd93b35e4b3f5d1c9da563133dbc862cc
sio:SIO_000628
miriam-gene:64240
,
lld:C0947622
;
a
sio:SIO_001121
.
}
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_provenance
{
dgn-np:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_assertion
dcterms:description
"[To investigate a possible association between transporter gene polymorphism and gallstone formation, we examined five common polymorphisms in the ABCG5 (Q604E) and ABCG8 (D19H, Y54C, T400K, A632V) genes in patients with gallstone disease (GS).]. 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:17612515
;
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:NP257445.RAMOWgDYOvn15SXyfDBan9XDprwvQL8s2PoQ9yPmQKClc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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
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"v2.1.0" .
}