@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0
> .
@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:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_head
{
this:
np:hasAssertion
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion
;
np:hasProvenance
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance
;
np:hasPublicationInfo
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion
a
np:Assertion
.
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance
a
np:Provenance
.
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion
{
miriam-gene:23025
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN2722972debd72201e0d71ed78e8a57c6
sio:SIO_000628
miriam-gene:23025
,
lld:C0002736
;
a
sio:SIO_001122
.
}
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_provenance
{
dgn-np:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_assertion
dcterms:description
"[The common variant rs12608932, located within an intron of UNC13A gene on chromosome 19p13.3, has been suggested to influence susceptibility to amyotrophic lateral sclerosis (ALS), as well as survival, in patients of north European descent.]. 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:22921269
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP867047.RAIB_bvfpRDaQ36NEeDWXhCQ1VMq9VNdMSmI7382ELeF0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:27+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" .
}