@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg
> .
@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:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_head
{
this:
np:hasAssertion
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion
;
np:hasProvenance
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance
;
np:hasPublicationInfo
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion
a
np:Assertion
.
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance
a
np:Provenance
.
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion
{
miriam-gene:7415
a
ncit:C16612
.
lld:C1368019
a
ncit:C7057
.
dgn-gda:DGNfebb6eb712252096ecbc3a70ef3335ea
sio:SIO_000628
miriam-gene:7415
,
lld:C1368019
;
a
sio:SIO_001121
.
}
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_provenance
{
dgn-np:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_assertion
dcterms:description
"[Mutations in valosin-containing protein (VCP) gene, already known to be associated with the multisystemic disorder, inclusion body myopathy with Paget's disease and frontotemporal dementia (IBMPFD), have been recently found also in familial cases of amyotrophic lateral sclerosis (ALS).]. 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:22137929
;
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:NP276484.RABiAdC4bFoqckd80preFdeP8MlEeVheMVh9-R9BZ4Clg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}