@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI
> .
@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:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_head
{
this:
np:hasAssertion
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_assertion
;
np:hasProvenance
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_provenance
;
np:hasPublicationInfo
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_assertion
a
np:Assertion
.
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_provenance
a
np:Provenance
.
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGNe12827d7666b48b678692965b8d31a1f
sio:SIO_000628
miriam-gene:24
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_provenance
{
dgn-np:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_assertion
dcterms:description
"[Genes implicated in monogenic macular dystrophies are good candidate susceptibility genes for ARMD, although to date, with the possible exception of ABCA4, none of these genes have been shown to confer increased risk of ARMD.]. 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:12960208
;
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:NP173065.RAHQxgB8cz_28jLtQ80DzsLTksPLW950ykTMkK2_NiuwI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}