@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA
> .
@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:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_head
{
this:
np:hasAssertion
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_assertion
;
np:hasProvenance
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_provenance
;
np:hasPublicationInfo
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_assertion
a
np:Assertion
.
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_provenance
a
np:Provenance
.
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_assertion
{
miriam-gene:4018
a
ncit:C16612
.
lld:C0454582
a
ncit:C7057
.
dgn-gda:DGNb30efbb49c1358ae409ad613cc463780
sio:SIO_000628
miriam-gene:4018
,
lld:C0454582
;
a
sio:SIO_001121
.
}
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_provenance
{
dgn-np:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_assertion
dcterms:description
"[Certain prominent features of this case (in particular, the profile of semantic impairment) have not been emphasised in previous descriptions of LPA or PNFA, suggesting that GRN may cause an overlapping PPA syndrome but with a distinctive cognitive profile.]. 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:19766663
;
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:NP853406.RA_kJUUA_RwUdnZIsaT1VAUmH7fTMxhEvZ2cON5Zg3zRA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}