@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs
> .
@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:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_head
{
this:
np:hasAssertion
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_assertion
;
np:hasProvenance
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_provenance
;
np:hasPublicationInfo
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_assertion
a
np:Assertion
.
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_provenance
a
np:Provenance
.
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0338437
a
ncit:C7057
.
dgn-gda:DGN0686aa2606c3736e155cc503fd6aef17
sio:SIO_000628
miriam-gene:3918
,
lld:C0338437
;
a
sio:SIO_001121
.
}
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_provenance
{
dgn-np:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_assertion
dcterms:description
"[The Ts8B2 ELISA is particularly useful for the diagnosis of active as opposed to inactive cases of NCC and conduct of the assay is also facilitated by the fact that assay sensitivity is significantly greater when serum as opposed to CSF samples are employed.]. 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:19712705
;
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:NP261263.RAgkUYe8WBfbm1fbk_CNEkhhJMfomc1XArySuY_NYJwRs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}