@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA
> .
@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:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_head
{
this:
np:hasAssertion
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion
;
np:hasProvenance
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance
;
np:hasPublicationInfo
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion
a
np:Assertion
.
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance
a
np:Provenance
.
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0029134
a
ncit:C7057
.
dgn-gda:DGN7b683a671c05249df58acac994e00928
sio:SIO_000628
miriam-gene:3918
,
lld:C0029134
;
a
sio:SIO_001121
.
}
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_provenance
{
dgn-np:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_assertion
dcterms:description
"[The cerebrospinal fluid (CSF) and serum from 64 patients with multiple sclerosis (MS) and 47 patients with monosymptomatic optic neuritis (ON) were analyzed for the distribution of allotypic determinants on IgG and compared to similar samples from 51 patients with other neurological diseases (OND) as well as to serum samples from 97 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:6713741
;
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:NP459853.RACoMxaA3NTkkUJhgJglC_8g-xWGaLGbs4u0zCSpYFMtA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}