@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_head
{
this:
np:hasAssertion
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_assertion
;
np:hasProvenance
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_provenance
;
np:hasPublicationInfo
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_assertion
a
np:Assertion
.
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_provenance
a
np:Provenance
.
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_assertion
{
miriam-gene:4137
a
ncit:C16612
.
lld:C0751072
a
ncit:C7057
.
dgn-gda:DGNdbd5822d072e89630690559ab6e07b5e
sio:SIO_000628
miriam-gene:4137
,
lld:C0751072
;
a
sio:SIO_001122
.
}
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_provenance
{
dgn-np:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_assertion
dcterms:description
"[ Clinical subtypes of FTLD have different tau and APOE genotype frequencies, suggesting these genes may influence the clinical presentation. Further studies should be performed to confirm this finding and to see if the pathologic phenotypes are also assoc]. 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:11939896
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP79086.RARt9uEK3Scn7IP-IagMZbQ918bQVjgAkW3WByCywwJNU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:23+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}