@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY
> .
@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:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_head
{
this:
np:hasAssertion
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_assertion
;
np:hasProvenance
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_provenance
;
np:hasPublicationInfo
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_assertion
a
np:Assertion
.
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_provenance
a
np:Provenance
.
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0154723
a
ncit:C7057
.
dgn-gda:DGNf22a427f20d607cb0fca44c72d72c378
sio:SIO_000628
miriam-gene:2099
,
lld:C0154723
;
a
sio:SIO_001121
.
}
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_provenance
{
dgn-np:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_assertion
dcterms:description
"[In a case-control study, including 210 Caucasoid migraine patients and 210 controls, we examined association between three single nucleotide polymorphisms in the coding region of ESR1, rs2077642, rs1801132, and rs2228480, and an Alu insertion in PGR, and migraine, migraine without aura or migraine with aura.]. 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:19175383
;
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:NP556352.RADVlwIR0o3muhrEPWvD6o1_2oGEFUrJQ8HMl4g_E2nFY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:35+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" .
}