@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs
> .
@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:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_head
{
this:
np:hasAssertion
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion
;
np:hasProvenance
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance
;
np:hasPublicationInfo
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion
a
np:Assertion
.
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance
a
np:Provenance
.
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C2936349
a
ncit:C7057
.
dgn-gda:DGN1939b06abeb0826adb98817dfd23daac
sio:SIO_000628
miriam-gene:5621
,
lld:C2936349
;
a
sio:SIO_001121
.
}
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_provenance
{
dgn-np:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_assertion
dcterms:description
"[Six cases had a mutation at codon 102 of the prion protein (PrP) gene and in these the characteristic pathology was the formation of multicentric amyloid plaques which were stained with PrP antibody, whereas spongiform changes were absent in one and minimal in two.]. 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:8355811
;
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:NP287932.RAZQP8yvhSjSuf9Gr7A9QhYfn8opuoHonAVc0ZVb8WDWs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}