@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw
> .
@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:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_head
{
this:
np:hasAssertion
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_assertion
;
np:hasProvenance
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_assertion
a
np:Assertion
.
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_provenance
a
np:Provenance
.
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0022336
a
ncit:C7057
.
dgn-gda:DGNea8d95483c15a7c757e87549362ccd9c
sio:SIO_000628
miriam-gene:5621
,
lld:C0022336
;
a
sio:SIO_001121
.
}
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_provenance
{
dgn-np:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_assertion
dcterms:description
"[A broadening spectrum of human prion diseases has now been identified including novel entities such as Fatal Familial Insomnia and variants of CJD and GSS characterised by specific abnormalities in the human prion protein (PrP) gene on chromosome 20.]. 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:8841969
;
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:NP1359180.RAasYIFeDbA9X2l9El9lOL7iMDJit-PDExLWHNsFg5YNw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:02+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" .
}