@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs
> .
@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:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_head
{
this:
np:hasAssertion
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_assertion
;
np:hasProvenance
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_provenance
;
np:hasPublicationInfo
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_assertion
a
np:Assertion
.
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_provenance
a
np:Provenance
.
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_assertion
{
miriam-gene:4976
a
ncit:C16612
.
lld:C0152136
a
ncit:C7057
.
dgn-gda:DGN099fb1460078fc2226b636cf94c5e383
sio:SIO_000628
miriam-gene:4976
,
lld:C0152136
;
a
sio:SIO_001121
.
}
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_provenance
{
dgn-np:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_assertion
dcterms:description
"[Results suggested that genetic variation in five of the candidate genes (RDX, SNX16, OPA1, SOD2 and CYP1B1) is unlikely to confer major risk to develop normal tension glaucoma in the German population.]. 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:19754948
;
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:NP763185.RATl8i2bOtzVdL5CKKNpiYjNLFWWLOMfcRZwHdO9mxDTs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:31+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" .
}