@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE
> .
@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:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_head
{
this:
np:hasAssertion
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_assertion
;
np:hasProvenance
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_provenance
;
np:hasPublicationInfo
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_assertion
a
np:Assertion
.
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_provenance
a
np:Provenance
.
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_assertion
{
miriam-gene:4035
a
ncit:C16612
.
lld:C0085400
a
ncit:C7057
.
dgn-gda:DGN32d5cdb9ac0a92d194964c209e70b8f7
sio:SIO_000628
miriam-gene:4035
,
lld:C0085400
;
a
sio:SIO_001121
.
}
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_provenance
{
dgn-np:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_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:NP776638.RA002Gycwf3x2zmpylNaDOUBWBbHvw7QISPxpKURgdqcE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}