@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk
> .
@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:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_head
{
this:
np:hasAssertion
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_assertion
;
np:hasProvenance
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_provenance
;
np:hasPublicationInfo
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_assertion
a
np:Assertion
.
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_provenance
a
np:Provenance
.
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGNc628e80918c9da63c85dfcb821e690d3
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_provenance
{
dgn-np:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_assertion
dcterms:description
"[A common polymorphism (Met or Val) at codon 129 of the PrP gene (PRNP) features prominently in the risk and phenotype, of prion disease, and an abnormality in its distribution frequency may signal a role for PrP in other diseases.]. 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:16315279
;
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:NP524382.RAPDBtDRcNc_Yj-okg_3GV9j2pXpwQ3E7mcxm-cI9AWFk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:42+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" .
}