@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM
> .
@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:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_head
{
this:
np:hasAssertion
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion
;
np:hasProvenance
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion
a
np:Assertion
.
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance
a
np:Provenance
.
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion
{
miriam-gene:203228
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGN0b582b6738ab8fe51a459836a268e0b6
sio:SIO_000628
miriam-gene:203228
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_provenance
{
dgn-np:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_assertion
dcterms:description
"[There is a higher than expected incidence of parkinsonism in ALS patients with C9ORF72 expansions, and the G4C2 repeat has also been reported in other motor phenotypes, such as primary lateral sclerosis, progressive muscular atrophy, corticobasal syndrome and Huntington-like disorders.]. 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:24493408
;
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:NP1151873.RAqm8TwgKU0TEJS0Z7HRaCAV4ovRruqKWCftnj2g909IM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:28+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" .
}