@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA
> .
@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:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_head
{
this:
np:hasAssertion
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_assertion
;
np:hasProvenance
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_assertion
a
np:Assertion
.
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_provenance
a
np:Provenance
.
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0456909
a
ncit:C7057
.
dgn-gda:DGNa07a281725fe3ca31f770fcd97b66909
sio:SIO_000628
miriam-gene:3075
,
lld:C0456909
;
a
sio:SIO_001121
.
}
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_provenance
{
dgn-np:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_assertion
dcterms:description
"[Age related macular degeneration (AMD) is a common form of blindness in the western world and genetic variations of several complement genes, including the complement regulator Factor H, the central complement component C3, Factor B, C2, and also Factor I confer a risk for the disease.]. 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:20711704
;
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:NP772309.RAYr88rVHFawuP16BJRPSBgpaiFy4DFVm1T57dYjAriyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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" .
}