@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE
> .
@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:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_head
{
this:
np:hasAssertion
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_assertion
;
np:hasProvenance
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_provenance
;
np:hasPublicationInfo
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_assertion
a
np:Assertion
.
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_provenance
a
np:Provenance
.
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0281267
a
ncit:C7057
.
dgn-gda:DGNc33939de36397cfda37a247ef3600691
sio:SIO_000628
miriam-gene:1588
,
lld:C0281267
;
a
sio:SIO_001121
.
}
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_provenance
{
dgn-np:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_assertion
dcterms:description
"[However, a 3-bp deletion/insertion CYP19 polymorphism, which is located in the same intron approximately 50 bp upstream to the (TTTA)n repeat, was evidently associated with the menopausal status in both the BC and biBC cohorts.]. 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:12204674
;
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:NP402648.RAYgbOOmAPq889LuDufN3BHlBwrsrJOI2Tc9ijLiqSrOE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}