@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY
> .
@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/v4.0.0/void/
> .
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_head
{
this:
np:hasAssertion
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_assertion
;
np:hasProvenance
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_assertion
a
np:Assertion
.
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_provenance
a
np:Provenance
.
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN07eee7470d5aec1c8f71970e517c330d
sio:SIO_000628
miriam-gene:1545
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_provenance
{
dgn-np:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_assertion
dcterms:description
"[To evaluate the prevalence and the diagnostic utility of testing for CYP1B1 copy number variation (CNV) in primary congenital glaucoma (PCG) cases unexplained by CYP1B1 point mutations in The Australian and New Zealand Registry of Advanced Glaucoma.]. 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:25750510
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1269524.RAcQVpkyx8LT3MDEYRJItAW2a0mlE1ua6pycwsv_ZgaTY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:21+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}