@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM
> .
@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:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_head
{
this:
np:hasAssertion
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_assertion
;
np:hasProvenance
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_provenance
;
np:hasPublicationInfo
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_assertion
a
np:Assertion
.
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_provenance
a
np:Provenance
.
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN9e72f7b86fc01544b0cdb9de16192b5b
sio:SIO_000628
miriam-gene:2100
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_provenance
{
dgn-np:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_assertion
dcterms:description
"[To investigate genetic single nucleotide polymorphisms (SNPs) in estrogen receptor-α (ERα) (ESR1, rs2234693, rs1801132, rs7757956 and rs2813544) and ERβ (ESR2, rs3020450, rs7154455 and rs4986938) genes and relate them to the adverse effects lipodystrophy, dyslipidemia and metabolic syndrome as well as to differences in their prevalence between sexes in HIV-infected individuals on HAART.]. 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:22011627
;
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:NP772552.RAG3cLkOztbQjyy5RWxKMFSA6lt-sQDi-bpInLFk57bVM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}