@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks
> .
@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:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_head
{
this:
np:hasAssertion
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_assertion
;
np:hasProvenance
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_provenance
;
np:hasPublicationInfo
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_assertion
a
np:Assertion
.
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_provenance
a
np:Provenance
.
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_assertion
{
miriam-gene:4594
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGNe52e034fcc7a8b9e56e6c01418ff461d
sio:SIO_000628
miriam-gene:4594
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_provenance
{
dgn-np:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_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:NP760103.RAKDDl8m3rx_uwI-gg3aPihdBU5Kn2CQ_CckmrH4k27Ks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}