@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos
> .
@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:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_head
{
this:
np:hasAssertion
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_assertion
;
np:hasProvenance
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_provenance
;
np:hasPublicationInfo
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_assertion
a
np:Assertion
.
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_provenance
a
np:Provenance
.
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0036202
a
ncit:C7057
.
dgn-gda:DGNf701a8c82b2b8de7c69c4e37936b4ea6
sio:SIO_000628
miriam-gene:1594
,
lld:C0036202
;
a
sio:SIO_001121
.
}
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_provenance
{
dgn-np:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_assertion
dcterms:description
"[Variants of selected polymorphisms: -1260/ C>A in CYP27B1, Lys198Asn in EDN1, and Ile105Val in GSTP1, were examined to determine if they confer susceptibility to sarcoidosis, based on an analysis of 180 Slovenian patients in comparison with 283 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:20082271
;
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:NP801736.RAQUPnPJ8WqFxAd4Dc4BdSqpp5tiQj2XwaQa8CKAGBjos130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}