@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I
> .
@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:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_head
{
this:
np:hasAssertion
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_assertion
;
np:hasProvenance
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_assertion
a
np:Assertion
.
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_provenance
a
np:Provenance
.
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C2931859
a
ncit:C7057
.
dgn-gda:DGN23243cf3107f756a53be2e0f365b3257
sio:SIO_000628
miriam-gene:5621
,
lld:C2931859
;
a
sio:SIO_001121
.
}
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_provenance
{
dgn-np:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_assertion
dcterms:description
"[Furthermore, polymorphic codon 129 of the PRNP gene encodes either methionine or valine and appears to influence the susceptibility of patients to iatrogenic and sporadic CJD as well as the neuropathological phenotype in these forms of CJD.]. 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:15449458
;
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:NP462137.RAEdVfzHF_jqLnENn_C6li8LTx3hdr-ZB9WH35BiecK7I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:14+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" .
}