@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs
> .
@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:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_head
{
this:
np:hasAssertion
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_assertion
;
np:hasProvenance
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_provenance
;
np:hasPublicationInfo
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_assertion
a
np:Assertion
.
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_provenance
a
np:Provenance
.
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGNb5b24a5562652035565ced057825bc58
sio:SIO_000628
miriam-gene:1543
,
lld:C0009404
;
a
sio:SIO_001122
.
}
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_provenance
{
dgn-np:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_assertion
dcterms:description
"[Carriers of the A allele of the C4887A polymorphism have enhanced estrogen catabolism and lower free estradiol. Our results suggest, however, that inherent estrogen metabolism as determined by C4887A polymorphisms is not associated with CRN risk.]. 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:20094781
;
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:NP88885.RA2cri9eY7UU_4rVgy6JpV8WQvurtaC3pBbJ1XvhVZTxs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}