@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8
> .
@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:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_head
{
this:
np:hasAssertion
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion
;
np:hasProvenance
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance
;
np:hasPublicationInfo
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion
a
np:Assertion
.
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance
a
np:Provenance
.
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion
{
miriam-gene:54209
a
ncit:C16612
.
lld:C0494463
a
ncit:C7057
.
dgn-gda:DGN8402e03f05162391b4ce66f436665758
sio:SIO_000628
miriam-gene:54209
,
lld:C0494463
;
a
sio:SIO_001121
.
}
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_provenance
{
dgn-np:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_assertion
dcterms:description
"[The reduced function of TREM2 was speculated to be the main cause in the pathogenic effects of this risk variant, and TREM2 is highly expressed in white matter, as well as in the hippocampus and neocortex, which is partly consistent with the pathological features reported in AD brain, indicating the possible involvement of TREM2 in AD pathogenesis.]. 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:23407992
;
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:NP286477.RAeSUvn9hHhRffxg4S0SSJnQc1jeVdtOvsm7x4KRP1-s8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:41+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" .
}