@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA
> .
@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:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_head
{
this:
np:hasAssertion
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion
;
np:hasProvenance
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance
;
np:hasPublicationInfo
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion
a
np:Assertion
.
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance
a
np:Provenance
.
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0393570
a
ncit:C7057
.
dgn-gda:DGNe0e8eb3be536b2c4670417ac47e1a2b7
sio:SIO_000628
miriam-gene:4137
,
lld:C0393570
;
a
sio:SIO_001121
.
}
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_provenance
{
dgn-np:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_assertion
dcterms:description
"[We also observed suggestive association between AD and the marker rs9468, which defines the H1 haplotype, an extended haplotype that spans the MAPT gene and has previously been implicated in other neurodegenerative disorders including Parkinson's disease, progressive supranuclear palsy, and corticobasal degeneration.]. 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:22027014
;
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:NP290729.RADm4rsLmaH8W_lftVIfF8sbvDcmBYJSGsE4D36aYEEYA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
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"v2.1.0" .
}