@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA
> .
@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:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_head
{
this:
np:hasAssertion
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_assertion
;
np:hasProvenance
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_assertion
a
np:Assertion
.
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_provenance
a
np:Provenance
.
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0206368
a
ncit:C7057
.
dgn-gda:DGNed6223396eb538b39f729c494d5ba12b
sio:SIO_000628
miriam-gene:4313
,
lld:C0206368
;
a
sio:SIO_001121
.
}
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_provenance
{
dgn-np:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_assertion
dcterms:description
"[Therefore, equimolar amounts of DNA samples of 80 subjects with PEX syndrome, 80 with PEX glaucoma (PEXG) and 80 controls were combined into separate pools and hybridized to 500K SNP arrays (Affymetrix).]. 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:20808326
;
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:NP630250.RAtHR2yF2MCGbDTw-nTpQTPHLeqAO9wXBpcUSo7KOFzuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}