@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA
> .
@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:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_head
{
this:
np:hasAssertion
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion
;
np:hasProvenance
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance
;
np:hasPublicationInfo
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion
a
np:Assertion
.
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance
a
np:Provenance
.
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN1fa7eca816c399665abf3b22e8f46672
sio:SIO_000628
miriam-gene:3075
,
lld:C0242383
;
a
sio:SIO_001122
.
}
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_provenance
{
dgn-np:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_assertion
dcterms:description
"[Our findings indicate that the CFH gene is involved in the onset of AMD, whereas both, the CFH and ARMS2 genes, and more weakly, the HtrA1 gene, appear to account for the advancement of AMD.]. 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:19169232
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46885.RAbA1NdkL9kZD9bj4S48wpoByyWNg3AEFbl8oQXhVf2QA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}