@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA
> .
@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:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_head
{
this:
np:hasAssertion
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_assertion
;
np:hasProvenance
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_provenance
;
np:hasPublicationInfo
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_assertion
a
np:Assertion
.
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_provenance
a
np:Provenance
.
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_assertion
{
miriam-gene:718
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGNaaed6911af26e7a06ec5724f4f7b4e3e
sio:SIO_000628
miriam-gene:718
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_provenance
{
dgn-np:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP275623.RAQiCZlIKdNR9rWQSrUPz0w9HTW_rkC_RGnzrtCFqf7xA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:17+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" .
}