@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco
> .
@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:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_head
{
this:
np:hasAssertion
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_assertion
;
np:hasProvenance
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_provenance
;
np:hasPublicationInfo
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_assertion
a
np:Assertion
.
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_provenance
a
np:Provenance
.
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_assertion
{
miriam-gene:966
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNd78793e8e98ba3df590b1fa619c403e8
sio:SIO_000628
miriam-gene:966
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_provenance
{
dgn-np:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_assertion
dcterms:description
"[The presence of this glycation motif in human CD59, but not in CD59 of other species, may help explain the distinct propensity of humans to develop vascular proliferative complications of diabetes.]. 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:10805801
;
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:NP399049.RAPrQnFPBbBnsALtzfWOZrRuH1ngkqHUPJVJHqxGEKOco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}