@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE
> .
@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:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_head
{
this:
np:hasAssertion
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_assertion
;
np:hasProvenance
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_assertion
a
np:Assertion
.
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_provenance
a
np:Provenance
.
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_assertion
{
miriam-gene:5542
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN47633f83e5daed2ed59f12e0171fb17c
sio:SIO_000628
miriam-gene:5542
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_provenance
{
dgn-np:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_assertion
dcterms:description
"[Given its rarity, it is challenging to investigate the mechanisms that initiate MS in such young individuals and to assess whether PMS and adult MS share the same risk factors, rather than being 2 separate conditions.]. 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:24198289
;
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:NP799715.RAguf6wZ1fPXTowuLqUH8-OAdgt8H3_0hUp5Vk0zMhaWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}