@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU
> .
@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:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_head
{
this:
np:hasAssertion
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_assertion
;
np:hasProvenance
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_provenance
;
np:hasPublicationInfo
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_assertion
a
np:Assertion
.
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_provenance
a
np:Provenance
.
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_assertion
{
miriam-gene:4035
a
ncit:C16612
.
lld:C0333463
a
ncit:C7057
.
dgn-gda:DGNa43b3a5d22258f6124d2b8df9c30d2b7
sio:SIO_000628
miriam-gene:4035
,
lld:C0333463
;
a
sio:SIO_001121
.
}
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_provenance
{
dgn-np:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_assertion
dcterms:description
"[We reviewed the available clinical and neuropathological records for all six cases looking specifically for concordance and discordance of clinical phenotype, neuritic amyloid plaques (NP), neurofibrillary tangles (NFT) and Lewy related pathology (LRP).]. 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:17615170
;
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:NP870159.RAdQlu9QX93P7PquuAWDheIdbAyXnkrRY5WoChAs23bGU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}