@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E
> .
@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:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_head
{
this:
np:hasAssertion
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_assertion
;
np:hasProvenance
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_assertion
a
np:Assertion
.
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_provenance
a
np:Provenance
.
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_assertion
{
miriam-gene:4308
a
ncit:C16612
.
lld:C0007273
a
ncit:C7057
.
dgn-gda:DGN5a4a2b71b0c796b60cd9e32208cd7c2c
sio:SIO_000628
miriam-gene:4308
,
lld:C0007273
;
a
sio:SIO_001122
.
}
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_provenance
{
dgn-np:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_assertion
dcterms:description
"[The results from this GWAS generate hypotheses regarding several SNPs that may be associated with SCA phenotypes in multiple arterial beds. Given the number of tests conducted, subsequent independent replication in a staged approach is essential to identify genetic variants that may be implicated in atherosclerosis.]. 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:17903303
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP93978.RAvrBpXao6eGZU_NhhweZ3na4R30CVp6UD5Up7Xogsm2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
}