@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_head
{
this:
np:hasAssertion
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion
;
np:hasProvenance
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance
;
np:hasPublicationInfo
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion
a
np:Assertion
.
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance
a
np:Provenance
.
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGNf6513c559439eb0462d370791ce2bcd3
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001122
.
}
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_provenance
{
dgn-np:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_assertion
dcterms:description
"[Indeed, the phenotypical expression of two of the most common mutations in the human PRNP gene associated with genetic prion diseases, D178N and E200K, is clearly modulated by the codon 129 polymorphism.]. 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:19684471
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP757874.RARzMZui39x0FAFaI253Z6xiVtxiQHzLCWxdZVPmmqCNs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:28+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}