@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM
> .
@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:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_head
{
this:
np:hasAssertion
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_assertion
;
np:hasProvenance
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_provenance
;
np:hasPublicationInfo
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_assertion
a
np:Assertion
.
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_provenance
a
np:Provenance
.
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_assertion
{
miriam-gene:5654
a
ncit:C16612
.
lld:C0017921
a
ncit:C7057
.
dgn-gda:DGN60fe7c2eff730c3380a16cc3514be85a
sio:SIO_000628
miriam-gene:5654
,
lld:C0017921
;
a
sio:SIO_001121
.
}
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_provenance
{
dgn-np:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_assertion
dcterms:description
"[We tested whether these SNPs are associated with AMD in Israeli populations, if they underlie variable phenotype and response to therapy in neovascular AMD (NVAMD), and if HTRA1 expression in vivo is associated with its promoter variant.]. 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:19065273
;
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:NP164229.RAvSVuWjCwxWWyxd9fHdP4Y5wTD6AkMACsyRzRvOUMAkM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}