@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0
> .
@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:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_head
{
this:
np:hasAssertion
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_assertion
;
np:hasProvenance
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_assertion
a
np:Assertion
.
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_provenance
a
np:Provenance
.
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_assertion
{
miriam-gene:629
a
ncit:C16612
.
lld:C0017921
a
ncit:C7057
.
dgn-gda:DGN458118ba80a7d08996f70bcd3a27bb98
sio:SIO_000628
miriam-gene:629
,
lld:C0017921
;
a
sio:SIO_001121
.
}
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_provenance
{
dgn-np:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_assertion
dcterms:description
"[For incident AMD, all these variants except CFB were significantly related to progression to advanced AMD, after controlling for baseline AMD grade and other factors, with ORs from 1.8 to 4.0 for presence of two risk alleles and 0.4 for the protective allele.]. 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:19117936
;
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:NP333304.RAy1bv0BMhv8bBeUz_VIpEzOvWdDIPX1ac6WPdKGBpcK0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:16+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" .
}