@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang
> .
@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:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_head
{
this:
np:hasAssertion
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_assertion
;
np:hasProvenance
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_provenance
;
np:hasPublicationInfo
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_assertion
a
np:Assertion
.
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_provenance
a
np:Provenance
.
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_assertion
{
miriam-gene:154
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN60c80463f69eb7d796b55675f3b5f483
sio:SIO_000628
miriam-gene:154
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_provenance
{
dgn-np:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_assertion
dcterms:description
"[Our findings suggest that these tagging SNPs in HSD11B1 and IRS2 mark regions of the genome that may harbor risk alleles for breast cancer, and these associations are probably independent of adiposity.]. 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:18611262
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP49075.RACFPXHnWmwFlYdqGV8GFQoSN4gc3YKSrbSuOvriS3Ang130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}