@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI
> .
@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:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_head
{
this:
np:hasAssertion
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_assertion
;
np:hasProvenance
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_provenance
;
np:hasPublicationInfo
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_assertion
a
np:Assertion
.
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_provenance
a
np:Provenance
.
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_assertion
{
miriam-gene:6323
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGNc8e733f2f3c8fd43360d6a9bfb71a215
sio:SIO_000628
miriam-gene:6323
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_provenance
{
dgn-np:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_assertion
dcterms:description
"[Furthermore, whether the migraine of the mother could be influenced by her SCN1A mutation mosaicism is not known, but increased awareness of migraine in future studies of SCN1A related epilepsies could clarify this intriguing link between migraine and epilepsy.]. 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:19673951
;
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:NP605397.RAijmjacRIFQWZ6JVXylngav02MwU91WzSadr_-7_c8vI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}