@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM
> .
@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:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_head
{
this:
np:hasAssertion
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_assertion
;
np:hasProvenance
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_assertion
a
np:Assertion
.
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_provenance
a
np:Provenance
.
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0333559
a
ncit:C7057
.
dgn-gda:DGN8984085f510ff2a41f0b0f211839df55
sio:SIO_000628
miriam-gene:1636
,
lld:C0333559
;
a
sio:SIO_001121
.
}
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_provenance
{
dgn-np:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_assertion
dcterms:description
"[While this association was found to exist in the stroke subtype of lacunar infarction especially, the susceptibility of this genetic variant to the intracerebral hemorrhage (ICH) subtypes is unknown to date.]. 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:22999931
;
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:NP939657.RAyBudP7zQbLrkJQr0ESca2CSGuHU9fE4XqHbzWbypFXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}