@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4
> .
@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:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_head
{
this:
np:hasAssertion
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_assertion
;
np:hasProvenance
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_assertion
a
np:Assertion
.
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_provenance
a
np:Provenance
.
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_assertion
{
miriam-gene:3008
a
ncit:C16612
.
lld:C0038868
a
ncit:C7057
.
dgn-gda:DGNb1550a7363d396d835c400bea9c793cc
sio:SIO_000628
miriam-gene:3008
,
lld:C0038868
;
a
sio:SIO_001121
.
}
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_provenance
{
dgn-np:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_assertion
dcterms:description
"[These results are consistent with the hypothesis that a change either in the 5' or in the 3' flanking regions of the tau gene, or even other genes contained in the H1E haplotype, could increase the genetic susceptibility to PSP.]. 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:12112206
;
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:NP305416.RAmspZHoKNDfdKrHl9-cX3HN5qRY6v91OUO1WPJDImgF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}