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http://rdf.disgenet.org/nanopublications.trig#NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY
> .
@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:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_head
{
this:
np:hasAssertion
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_assertion
;
np:hasProvenance
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_assertion
a
np:Assertion
.
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_provenance
a
np:Provenance
.
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_assertion
{
miriam-gene:29978
a
ncit:C16612
.
lld:C0338451
a
ncit:C7057
.
dgn-gda:DGNcd3e6ef919016430d20aa986b8298a7f
sio:SIO_000628
miriam-gene:29978
,
lld:C0338451
;
a
sio:SIO_001121
.
}
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_provenance
{
dgn-np:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_assertion
dcterms:description
"[In particular, the progress in the molecular neuropathology with the discovery of pathogenic mutations in TAR DNA binding protein (TARDBP), fused in sarcoma (FUS), ubiquilin2 (UBQLN2) and most recently C9ORF72 (abbreviation for the open reading frame 72 on chromosome 9) has further substantiated the - clinically temporarily forgotten - relation of classic ALS to frontotemporal degeneration (FTD).]. 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:22918486
;
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:NP881333.RAKL2Dnp1Ew39Al5L4yl4QKDZOcUEVI79BX0BfLcsIyvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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
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}