@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk
> .
@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:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_head
{
this:
np:hasAssertion
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_assertion
;
np:hasProvenance
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_provenance
;
np:hasPublicationInfo
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_assertion
a
np:Assertion
.
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_provenance
a
np:Provenance
.
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C2349757
a
ncit:C7057
.
dgn-gda:DGNed7fb0781b147462581da0f9ebc599aa
sio:SIO_000628
miriam-gene:2688
,
lld:C2349757
;
a
sio:SIO_001121
.
}
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_provenance
{
dgn-np:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_assertion
dcterms:description
"[We tested DNA from 15 centrally infected cases of iatrogenic Creutzfeldt-Jakob disease (CJD) (dura mater or corneal homografts and stereotactic EEG electrodes), 11 peripherally infected cases (native human growth hormone or gonadotrophin), and 110 control individuals for the presence of mutations in the chromosome 20 amyloid gene.]. 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:8309577
;
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:NP338884.RA3EGl9WyAm6Qt-cG1wGT3W2utuKIiudiXNCzPRndy_Mk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}