@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow
> .
@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:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_head
{
this:
np:hasAssertion
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion
;
np:hasProvenance
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance
;
np:hasPublicationInfo
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion
a
np:Assertion
.
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance
a
np:Provenance
.
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion
{
miriam-gene:5819
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN34c3ed3cef9731c0ad6b76f9cdb3f79c
sio:SIO_000628
miriam-gene:5819
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_provenance
{
dgn-np:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_assertion
dcterms:description
"[the analysis of a very large data set suggests that genetic polymorphisms in PVRL2 may influence MS severity and supports the possibility that viral factors may contribute to the clinical course of MS, consistent with previous reports.]. 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:16738668
;
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:NP66395.RAX8EXAcqT4M6qqBUncP_UJMoNGxM42Pz3MWYJnVlU7ow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}