@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE
> .
@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:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_head
{
this:
np:hasAssertion
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_assertion
;
np:hasProvenance
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_provenance
;
np:hasPublicationInfo
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_assertion
a
np:Assertion
.
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_provenance
a
np:Provenance
.
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_assertion
{
miriam-gene:203228
a
ncit:C16612
.
lld:C0236642
a
ncit:C7057
.
dgn-gda:DGN6a529584ca6d0d83975f9902ff96ac9d
sio:SIO_000628
miriam-gene:203228
,
lld:C0236642
;
a
sio:SIO_001121
.
}
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_provenance
{
dgn-np:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_assertion
dcterms:description
"[Unlike most genes that are mutated in amyotrophic lateral sclerosis (ALS), which are ubiquitously expressed, the C9ORF72 ortholog was most highly transcribed in the neuronal populations that are sensitive to degeneration in ALS and frontotemporal dementia.]. 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:24185425
;
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:NP398410.RAxfPXF-6dtQlndnsBkuFzBvC2bFXT4oKfGSoW7TQlMeE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}