@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo
> .
@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:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_head
{
this:
np:hasAssertion
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_assertion
;
np:hasProvenance
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_provenance
;
np:hasPublicationInfo
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_assertion
a
np:Assertion
.
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_provenance
a
np:Provenance
.
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_assertion
{
miriam-gene:23435
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNe84c624c8f613e7eadc36f2a603a727f
sio:SIO_000628
miriam-gene:23435
,
lld:C0002736
;
a
sio:SIO_001122
.
}
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_provenance
{
dgn-np:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_assertion
dcterms:description
"[To further examine the frequency of mutations in TARDBP in sporadic ALS, 279 ALS cases and 806 neurologically normal control individuals of European descent were screened for sequence variants, copy number variants, genetic and haplotype association with disease.]. 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:18545701
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP81051.RAIcIcvTAirqi8-UgpNxzRfu79kvbCX-cMRmyUVjNDvwo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:40+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" .
}