@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0
> .
@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:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_head
{
this:
np:hasAssertion
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_assertion
;
np:hasProvenance
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_provenance
;
np:hasPublicationInfo
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_assertion
a
np:Assertion
.
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_provenance
a
np:Provenance
.
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_assertion
{
miriam-gene:6120
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN8e0bdf5ed3c39b0281f17169f7969d6b
sio:SIO_000628
miriam-gene:6120
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_provenance
{
dgn-np:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_assertion
dcterms:description
"[Although major abnormalities are seen in four functionally interrelated tissues, i.e., photoreceptors, retinal pigment epithelium (RPE), Bruch's membrane and choriocapillaries, the impairment of RPE cell functions is an early and crucial event in the molecular pathways leading to clinically relevant AMD changes.]. 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:16845209
;
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:NP173121.RAgd75eOx6XnODd90VMT0fTv2uo_xpG897lY12wOKv1n0130_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" .
}