@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_head
{
this:
np:hasAssertion
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_assertion
;
np:hasProvenance
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_provenance
;
np:hasPublicationInfo
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_assertion
a
np:Assertion
.
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_provenance
a
np:Provenance
.
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_assertion
{
miriam-gene:8929
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGNbd487afcb05d72119b0469999cc37ba3
sio:SIO_000628
miriam-gene:8929
,
lld:C0009324
;
a
sio:SIO_001122
.
}
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_provenance
{
dgn-np:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_assertion
dcterms:description
"[Genomic DNA from 2,833 Caucasian individuals including 854 patients with CD, 476 patients with UC, and 1,503 healthy unrelated controls was analyzed for SNPs in PHOX2B (rs16853571), NCF4 (rs4821544), and FAM92B (rs8050910), including rs224136 on chromosome 10q21.1.]. 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:19262523
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP88566.RAcA83rfqrYgxqUTyy8OyZH-0zHZBlcXt02WdO7rjJPSg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:29+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}