@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o
> .
@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/v3.0.0/void/
> .
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_head
{
this:
np:hasAssertion
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_assertion
;
np:hasProvenance
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_provenance
;
np:hasPublicationInfo
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_assertion
a
np:Assertion
.
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_provenance
a
np:Provenance
.
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_assertion
{
miriam-gene:5654
a
ncit:C16612
.
lld:C0008521
a
ncit:C7057
.
dgn-gda:DGN9c903cdacb8851ed48ecf7679be3da53
sio:SIO_000628
miriam-gene:5654
,
lld:C0008521
;
a
sio:SIO_001122
.
}
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_provenance
{
dgn-np:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_assertion
dcterms:description
"[The association pattern and haplotype estimation in the ARMS2/HTRA1 region of Japanese patients with PCV were very similar to those of Japanese patients with typical nAMD. The polymorphisms responsible for nAMD and PCV may be located in this region or in ]. 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:21191724
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP87930.RA7iMUSO45Z-MInS0SmYDOBvCQXi9u7KYk8_NquSgYn2o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:28+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}