@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk
> .
@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/v4.0.0/void/
> .
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_head
{
this:
np:hasAssertion
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_assertion
;
np:hasProvenance
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_assertion
a
np:Assertion
.
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_provenance
a
np:Provenance
.
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_assertion
{
miriam-gene:64321
a
ncit:C16612
.
lld:C0038525
a
ncit:C7057
.
dgn-gda:DGN7dd1f247306f8cfc5796da7fd8794156
sio:SIO_000628
miriam-gene:64321
,
lld:C0038525
;
a
sio:SIO_001121
.
}
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_provenance
{
dgn-np:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_assertion
dcterms:description
"[The combination of Sox17 deficiency and angiotensin II infusion in mice induces vascular abnormalities closely resembling the cardinal features of IA such as luminal dilation, wall thinning, tortuosity, and subarachnoid hemorrhages.]. 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:25596186
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1256215.RAPFKZ4NVFvHLNMOUD_7iYFnYz_A323HcRnIBQOBSyYWk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:15+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}