@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0
> .
@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/v3.0.0/void/
> .
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_head
{
this:
np:hasAssertion
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_assertion
;
np:hasProvenance
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_provenance
;
np:hasPublicationInfo
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_assertion
a
np:Assertion
.
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_provenance
a
np:Provenance
.
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0149931
a
ncit:C7057
.
dgn-gda:DGN3c287d74dd9bc88654d1c6bdcf0f168e
sio:SIO_000628
miriam-gene:4854
,
lld:C0149931
;
a
sio:SIO_001121
.
}
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_provenance
{
dgn-np:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_assertion
dcterms:description
"[Additional molecular insight into the pathophysiology of migraine may come from other monogenic syndromes (for instance cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, which is caused by NOTCH3 mutations), in which migraine is prominent.]. 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:19455354
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP596479.RA1Wx_wYK7M3HwKksrv_kS_zxdO-XcTJZ-2nYkOrcvnf0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:36+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}