@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI
> .
@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:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_head
{
this:
np:hasAssertion
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion
;
np:hasProvenance
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance
;
np:hasPublicationInfo
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion
a
np:Assertion
.
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance
a
np:Provenance
.
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNb2f079b409d9b5b1e1a7bf572c9f0778
sio:SIO_000628
miriam-gene:4137
,
lld:C0338451
;
a
sio:SIO_001122
.
}
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_provenance
{
dgn-np:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_assertion
dcterms:description
"[ This study of the largest series of patients with FTD confirms the primary role of tau in FTD and establishes that the H1 haplotype of the tau gene and the E2 allele of APOE interact by an unknown mechanism that increases the risk of FTD.]. 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:12056929
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61233.RAVvbH_vaCl8UQK36uKi7s0CoGtpXNxJ-MzLm8bIav4eI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}