@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs
> .
@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/v4.0.0/void/
> .
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_head
{
this:
np:hasAssertion
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_assertion
;
np:hasProvenance
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_provenance
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np:hasPublicationInfo
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_assertion
a
np:Assertion
.
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_provenance
a
np:Provenance
.
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_assertion
{
miriam-gene:5654
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN3b18b5df0314c037369dd6e4733c57c0
sio:SIO_000628
miriam-gene:5654
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_provenance
{
dgn-np:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_assertion
dcterms:description
"[We identified a sample of patients with neovascular AMD, that in previous studies had been shown to be at elevated risk for the disease through environmental factors such as cigarette smoking and genetic variants including the complement factor H gene (CFH) on chromosome 1q25 and variants in the ARMS2/HtrA serine peptidase 1 (HTRA1) gene(s) on chromosome 10q26.]. 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:21682878
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP902906.RAeVi8SoEPPq2h2x3uX3mPTPzr9eNwJhI0TN8DsTsJBqs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:33+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
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;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}