@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg
> .
@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:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_head
{
this:
np:hasAssertion
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_assertion
;
np:hasProvenance
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_provenance
;
np:hasPublicationInfo
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_assertion
a
np:Assertion
.
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_provenance
a
np:Provenance
.
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C1865285
a
ncit:C7057
.
dgn-gda:DGN64ac6c10ac8705bbf9b6e871dd5e5a57
sio:SIO_000628
miriam-gene:5290
,
lld:C1865285
;
a
sio:SIO_001121
.
}
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_provenance
{
dgn-np:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_assertion
dcterms:description
"[We aimed to ascertain whether family history of major congenital malformations (MCMs) was increased in women with epilepsy (WWE) compared to controls (spouses) and whether family history of MCM was associated with occurrence of MCM in the offspring.]. 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:18977119
;
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:NP504753.RAYnjvm4rqlBqcoSNJHZInqLc4oWjEVH_E7KolURqIsdg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}