@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk
> .
@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:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_head
{
this:
np:hasAssertion
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_assertion
;
np:hasProvenance
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_provenance
;
np:hasPublicationInfo
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_assertion
a
np:Assertion
.
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_provenance
a
np:Provenance
.
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_assertion
{
miriam-gene:5654
a
ncit:C16612
.
lld:C0600518
a
ncit:C7057
.
dgn-gda:DGNa52fb794838eb16fe818cec2ec8eaa18
sio:SIO_000628
miriam-gene:5654
,
lld:C0600518
;
a
sio:SIO_001122
.
}
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_provenance
{
dgn-np:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_assertion
dcterms:description
"[The SERPING1 gene is comprehensively investigated in this study (using three tSNPs), and its genetic variants are evaluated in the largest neovascular AMD cohort to date. The hypothesis that SERPING1 has a modest effect on the risk of neovascular AMD is s]. 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:20606025
;
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:NP87919.RAlkVvyscb_OFI5ub_f0EHu83nQFy59YeI7CAuFvF0_Lk130_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" .
}