@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI
> .
@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:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_head
{
this:
np:hasAssertion
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_assertion
;
np:hasProvenance
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_provenance
;
np:hasPublicationInfo
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_assertion
a
np:Assertion
.
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_provenance
a
np:Provenance
.
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_assertion
{
miriam-gene:25793
a
ncit:C16612
.
lld:C0242422
a
ncit:C7057
.
dgn-gda:DGNc8f788fd65ae1eefc784a544ecd7085b
sio:SIO_000628
miriam-gene:25793
,
lld:C0242422
;
a
sio:SIO_001121
.
}
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_provenance
{
dgn-np:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_assertion
dcterms:description
"[Understanding how FBXO7 mutations cause disease will shed further light on the molecular mechanisms of neurodegeneration, with potential implications also for more common forms of parkinsonism, such as Parkinson disease and multiple system atrophy.]. 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:19038853
;
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:NP706220.RAZOiw2n-5GNE68q1KydgPac77Y2m8kD4Fnsl2eUHfZZI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:05+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" .
}