@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY
> .
@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:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_head
{
this:
np:hasAssertion
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_assertion
;
np:hasProvenance
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_provenance
;
np:hasPublicationInfo
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_assertion
a
np:Assertion
.
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_provenance
a
np:Provenance
.
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0342342
a
ncit:C7057
.
dgn-gda:DGN4eaafef616179d222ec7efe58d161d1d
sio:SIO_000628
miriam-gene:3126
,
lld:C0342342
;
a
sio:SIO_001121
.
}
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_provenance
{
dgn-np:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_assertion
dcterms:description
"[We therefore looked for antibodies (Ab) against the CaSR in patients with sporadic idiopathic hypoparathyroidism and their association, if any, with the major histocompatibility complex (MHC) class II human leukocyte antigen (HLA)-DR haplotypes.]. 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:14713274
;
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:NP502517.RA3FkNQL5z1uw4AA1EebEbEhQIsM7R9C4_d3zh35GN9XY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}