@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g
> .
@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:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_head
{
this:
np:hasAssertion
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_assertion
;
np:hasProvenance
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_provenance
;
np:hasPublicationInfo
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_assertion
a
np:Assertion
.
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_provenance
a
np:Provenance
.
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0021368
a
ncit:C7057
.
dgn-gda:DGN3856082dfc50b2180f78478cb21154be
sio:SIO_000628
miriam-gene:3075
,
lld:C0021368
;
a
sio:SIO_001122
.
}
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_provenance
{
dgn-np:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_assertion
dcterms:description
"[This study confirmed associations of the Y402H CFH gene variant with AMD in nonwhite populations, but neither explained the lack of association between inflammatory factors and AMD in the cohort nor the basis for the observed differences in AMD prevalence]. 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:18538409
;
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:NP104334.RAi01lfO6RoZ3XeDPu4PBzxqEO1zFXJnLcGsFlGDYEh8g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:37+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" .
}