@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus
> .
@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:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_head
{
this:
np:hasAssertion
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion
;
np:hasProvenance
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance
;
np:hasPublicationInfo
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion
a
np:Assertion
.
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance
a
np:Provenance
.
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion
{
miriam-gene:203228
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGNd994d214af90109b651718d90a17f501
sio:SIO_000628
miriam-gene:203228
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_provenance
{
dgn-np:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_assertion
dcterms:description
"[This study determined the frequency of C9orf72 repeat expansions in different motor neuron diseases (amyotrophic lateral sclerosis (ALS), motor neuron diseases affecting primarily the first or the second motor neuron and hereditary spastic paraplegia).]. 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:24378086
;
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:NP1140616.RAI9Hg16DitwE4xk5phbR3paKJFy5Y9WFc-baT4lDYTus130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:23+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" .
}