@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE
> .
@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:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_head
{
this:
np:hasAssertion
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_assertion
;
np:hasProvenance
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_provenance
;
np:hasPublicationInfo
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_assertion
a
np:Assertion
.
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_provenance
a
np:Provenance
.
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_assertion
{
miriam-gene:1586
a
ncit:C16612
.
lld:C0016977
a
ncit:C7057
.
dgn-gda:DGN1e95ba11fd58b0cade9643575f9742dd
sio:SIO_000628
miriam-gene:1586
,
lld:C0016977
;
a
sio:SIO_001121
.
}
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_provenance
{
dgn-np:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_assertion
dcterms:description
"[The association of the CYP17 MspA1 polymorphism with an increased risk of gallbladder cancer, as well as biliary stones among overweight and diabetic individuals, suggests an interplay between genetic and hormonal risk factors in gallbladder disease.]. 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:16381022
;
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:NP181813.RAXvqvNeQd2j3fIM8JGcYKKKnTKGofYDKZDKYPIImyTlE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}