@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw
> .
@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:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_head
{
this:
np:hasAssertion
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_assertion
;
np:hasProvenance
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_provenance
;
np:hasPublicationInfo
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_assertion
a
np:Assertion
.
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_provenance
a
np:Provenance
.
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_assertion
{
miriam-gene:4155
a
ncit:C16612
.
lld:C0029134
a
ncit:C7057
.
dgn-gda:DGNd955f11b71384355cb4c1130b69321df
sio:SIO_000628
miriam-gene:4155
,
lld:C0029134
;
a
sio:SIO_001121
.
}
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_provenance
{
dgn-np:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_assertion
dcterms:description
"[We compared the DNA fragment frequencies of the two MBP regions in 34 patients suffering from multiple sclerosis and in 78 suffering from monosymptomatic idiopathic optic neuritis to those in 200 healthy controls.]. 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:9345452
;
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:NP431957.RAIAIUOj4XXL-goAQqh-nLMybhlL85jHbMgdEHMq5UPaw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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" .
}