@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w
> .
@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:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_head
{
this:
np:hasAssertion
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_assertion
;
np:hasProvenance
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_assertion
a
np:Assertion
.
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_provenance
a
np:Provenance
.
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0235031
a
ncit:C7057
.
dgn-gda:DGNd732d69465f38c068df34411911a859f
sio:SIO_000628
miriam-gene:5621
,
lld:C0235031
;
a
sio:SIO_001121
.
}
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_provenance
{
dgn-np:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_assertion
dcterms:description
"[To gain a better understanding of how mutations of the prion protein (PrP) gene are responsible for progressive dementia syndrome and to clarify the correlation between genotype and phenotype, which should help to explain how the prion promotes neurological symptoms.]. 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:12023426
;
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:NP788730.RAw3bFml2cAr6F7bo4ixORVO3O24TSjHxNvQ5JaODHW5w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:01+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" .
}