@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco
> .
@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:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_head
{
this:
np:hasAssertion
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion
;
np:hasProvenance
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance
;
np:hasPublicationInfo
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion
a
np:Assertion
.
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance
a
np:Provenance
.
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion
{
miriam-gene:5621
a
ncit:C16612
.
lld:C0022336
a
ncit:C7057
.
dgn-gda:DGN4a3274fb52e42df30f129c61c3aeb742
sio:SIO_000628
miriam-gene:5621
,
lld:C0022336
;
a
sio:SIO_001121
.
}
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_provenance
{
dgn-np:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_assertion
dcterms:description
"[Familial CJD accounts for approximately 10% of all European cases of CJD, and is associated with inherited mutations of the prion protein gene, caused by one of the 24 single amino acid substitutions or insertions of octapeptide repeats.]. 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:12064251
;
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:NP357765.RALgTdjsIhY1slBNbRbV2xaCOUNTc2ocUAlUONq9OLyco130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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" .
}