@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys
> .
@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:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_head
{
this:
np:hasAssertion
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion
;
np:hasProvenance
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance
;
np:hasPublicationInfo
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion
a
np:Assertion
.
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance
a
np:Provenance
.
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion
{
miriam-gene:2896
a
ncit:C16612
.
lld:C0085084
a
ncit:C7057
.
dgn-gda:DGN3499b88feefd36708a16c4d993f50b11
sio:SIO_000628
miriam-gene:2896
,
lld:C0085084
;
a
sio:SIO_001121
.
}
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_provenance
{
dgn-np:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_assertion
dcterms:description
"[Two hundred and twenty-three consecutive patients fulfilling clinical diagnostic criteria for frontotemporal lobar degeneration (FTLD), and 259 patients with motor neuron disease (MND), for whom genomic DNA was available, were investigated for the presence of mutations in tau (MAPT) and progranulin (PGRN) genes.]. 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:18192287
;
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:NP397557.RAFa_Zr8GKmI5XL9d2Lj4YKupLkUXThpuGkmOBmbNiyys130_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" .
}