@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_head
{
this:
np:hasAssertion
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_assertion
;
np:hasProvenance
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_provenance
;
np:hasPublicationInfo
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_assertion
a
np:Assertion
.
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_provenance
a
np:Provenance
.
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGN1ebd70da7000d4e231e1619039919e0f
sio:SIO_000628
miriam-gene:2099
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_provenance
{
dgn-np:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_assertion
dcterms:description
"[Interaction analysis of the PROGINS variant with our previously reported associated ESR1 594A variant showed that individuals who possessed at least one copy of both risk alleles were 3.2 times more likely to suffer migraine.]. 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:15654614
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP476533.RANpWCB8pyW42I09fU_2bMbrxeIq8WJYEzwwZZWCrlCcU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}