@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg
> .
@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:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_head
{
this:
np:hasAssertion
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_assertion
;
np:hasProvenance
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_assertion
a
np:Assertion
.
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_provenance
a
np:Provenance
.
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0085220
a
ncit:C7057
.
dgn-gda:DGNb6f73e035e407316d6177a48ad8019e0
sio:SIO_000628
miriam-gene:1636
,
lld:C0085220
;
a
sio:SIO_001121
.
}
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_provenance
{
dgn-np:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_assertion
dcterms:description
"[The apoE4 targeted replacement mice do not harbor any mutation in the amyloid precursor protein gene and, therefore, are similar to the majority of humans susceptible to cerebral amyloid angiopathy and ICH, where the APOE genetic polymorphism is the only known genetic risk factor.]. 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:18755411
;
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:NP413006.RARfdgm-qpKMBQonxen9qTxnt4IkXKwCh7GpPp99c-xEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}