@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ
> .
@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:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_head
{
this:
np:hasAssertion
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_assertion
;
np:hasProvenance
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_assertion
a
np:Assertion
.
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_provenance
a
np:Provenance
.
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0236075
a
ncit:C7057
.
dgn-gda:DGN4647cd555c8d188dc411761c1a8ba967
sio:SIO_000628
miriam-gene:1545
,
lld:C0236075
;
a
sio:SIO_001121
.
}
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_provenance
{
dgn-np:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_assertion
dcterms:description
"[This study aims to investigate the incidence of menopausal symptoms among midlife women according to their menopausal status, and to evaluate the contribution to their manifestation from CYP1B1 Leu432Val polymorphism as a predisposing factor for menopausal symptoms.]. 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:23350153
;
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:NP169259.RA66jX-TvTZlqwoStjW_M11LD4UxWETXrS0KdReYEcGCQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}