@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo
> .
@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:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_head
{
this:
np:hasAssertion
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_assertion
;
np:hasProvenance
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_provenance
;
np:hasPublicationInfo
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_assertion
a
np:Assertion
.
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_provenance
a
np:Provenance
.
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_assertion
{
miriam-gene:203228
a
ncit:C16612
.
lld:C0751072
a
ncit:C7057
.
dgn-gda:DGN87e2082ae2c1c2ebb9dc06049acfa168
sio:SIO_000628
miriam-gene:203228
,
lld:C0751072
;
a
sio:SIO_001121
.
}
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_provenance
{
dgn-np:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_assertion
dcterms:description
"[These findings corroborate the clinical importance of the C9ORF72 mutation in frontotemporal lobar degeneration, delineate phenotypic and neuropathological features that could help to guide genetic testing, and suggest hypotheses for elucidating the neurobiology of a culprit subcortical network.]. 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:22366791
;
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:NP963451.RAzhGA1jhBAdqWk2Bu4jVD6E4Ul02GKWIZCusSdwnAExo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:01+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" .
}