@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g
> .
@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:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_head
{
this:
np:hasAssertion
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_assertion
;
np:hasProvenance
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_assertion
a
np:Assertion
.
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_provenance
a
np:Provenance
.
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_assertion
{
miriam-gene:358
a
ncit:C16612
.
lld:C0011884
a
ncit:C7057
.
dgn-gda:DGNf0d99abb34d1b61aa9478789ed98bbbb
sio:SIO_000628
miriam-gene:358
,
lld:C0011884
;
a
sio:SIO_001121
.
}
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_provenance
{
dgn-np:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_assertion
dcterms:description
"[Hypoxia is thought to be a common precursor to neovascularization in many retinal diseases, including diabetic retinopathy, and therefore we analyzed the expression pattern and function of AQP1 in human retinal vascular endothelial cells cultured under hypoxic conditions.]. 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:18275976
;
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:NP188881.RAt8-zo_ur5tIhNkaK6ioP0tkmp7n-K_UMah7k7AsYV5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}