@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI
> .
@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:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_head
{
this:
np:hasAssertion
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_assertion
;
np:hasProvenance
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_provenance
;
np:hasPublicationInfo
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_assertion
a
np:Assertion
.
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_provenance
a
np:Provenance
.
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_assertion
{
miriam-gene:30813
a
ncit:C16612
.
lld:C0339284
a
ncit:C7057
.
dgn-gda:DGN12cf499e50194cddbc5af4a239adeffd
sio:SIO_000628
miriam-gene:30813
,
lld:C0339284
;
a
sio:SIO_001122
.
}
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_provenance
{
dgn-np:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_assertion
dcterms:description
"[Therefore, although we report a number of novel polymorphisms in the VSX1 and ID1 genes, the failure to identify any sequence variants that sort with the disease phenotype suggests that other genetic factors are involved in PPCD.]. 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:15725882
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP896022.RACdh-fDahQFZC3CX2u88ZLK3NuaS0vmZ6HUrSQ3jh2hI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:46+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" .
}