@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s
> .
@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/v4.0.0/void/
> .
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_head
{
this:
np:hasAssertion
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_assertion
;
np:hasProvenance
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_assertion
a
np:Assertion
.
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_provenance
a
np:Provenance
.
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN3fb0309c1358f69eaf53dc06621fd562
sio:SIO_000628
miriam-gene:5621
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_provenance
{
dgn-np:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_assertion
dcterms:description
"[We developed gene panel based technologies to assess 16 genes known to harbour mutations causal of dementia and combined these with PCR based assessments of the C9orf72 hexanucleotide repeat expansion and the octapeptide repeat region of PRNP.]. 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:23998997
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1107209.RAs2bhM1Nt7sw37kcWG2nXGqKJtGgP8lqLTsjc2V1uV1s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:07+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}