@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw
> .
@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:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_head
{
this:
np:hasAssertion
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_assertion
;
np:hasProvenance
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_assertion
a
np:Assertion
.
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_provenance
a
np:Provenance
.
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_assertion
{
miriam-gene:11235
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN3c440b8c5a04cbca5b7e1d022db4c954
sio:SIO_000628
miriam-gene:11235
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_provenance
{
dgn-np:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_assertion
dcterms:description
"[Mutations in the essential adaptor proteins CCM2 or CCM3 lead to cerebral cavernous malformations (CCM), vascular lesions that most frequently occur in the brain and are strongly associated with hemorrhagic stroke, seizures, and other neurological disorders.]. 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:25825518
;
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:NP1275022.RAGv2y4iK9vw_vaqzwahUz17qPUXCGSvgqAzHhZKHbgRw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:24+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" .
}