@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik
> .
@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:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_head
{
this:
np:hasAssertion
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion
;
np:hasProvenance
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance
;
np:hasPublicationInfo
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion
a
np:Assertion
.
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance
a
np:Provenance
.
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0162534
a
ncit:C7057
.
dgn-gda:DGN1ccfa2b103a6004db2c2d985ff64e041
sio:SIO_000628
miriam-gene:5621
,
lld:C0162534
;
a
sio:SIO_001121
.
}
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_provenance
{
dgn-np:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_assertion
dcterms:description
"[The main cause for the development of transmissible spongiform encephalopathies (TSE) is the conformational change of prion protein from the normal cellular isoform (PrP(C)) into the abnormal isoform, named prion (PrP(Sc)).]. 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:17884181
;
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:NP631138.RAtmoAoJHOGmQLJUByFav6hZnJGW_YeWeoBgObRNhPdik130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:31+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" .
}