@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0
> .
@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:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_head
{
this:
np:hasAssertion
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_assertion
;
np:hasProvenance
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_provenance
;
np:hasPublicationInfo
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_assertion
a
np:Assertion
.
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_provenance
a
np:Provenance
.
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN67be0cb00140a55f725b11798fe8f28a
sio:SIO_000628
miriam-gene:4137
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_provenance
{
dgn-np:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_assertion
dcterms:description
"[MAPT-H1/H1 MCI carriers showed an increased bilateral atrophy in superior frontal gyri (including frontal eye fields and left prefrontal cortex) and precentral gyrus but also unilateral left atrophy in the inferior temporal gyrus and calcarine gyrus.]. 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:23064258
;
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:NP628103.RADXAqXttdtSc0QtWeUMgFSMSnbijAx6RXuS4GJgwLQh0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}