@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ
> .
@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:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_head
{
this:
np:hasAssertion
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion
;
np:hasProvenance
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion
a
np:Assertion
.
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance
a
np:Provenance
.
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion
{
miriam-gene:907
a
ncit:C16612
.
lld:C0339573
a
ncit:C7057
.
dgn-gda:DGNa56eddc79c0fffb332e0ca4c6fdf4dd7
sio:SIO_000628
miriam-gene:907
,
lld:C0339573
;
a
sio:SIO_001121
.
}
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_provenance
{
dgn-np:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_assertion
dcterms:description
"[One approach to identify genes that contribute to common complex ocular disorders such as primary open angle glaucoma (POAG) is to study the genetic determinates of endophenotypes that are defined by underlying pre-disposing heritable quantitative traits such as central corneal thickness (CCT).]. 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:21139683
;
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:NP776254.RA1B_PvkoXACF8_IfIblTDCn5gY5z3dVvTjY74VqxMOdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}