@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U
> .
@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:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_head
{
this:
np:hasAssertion
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_assertion
;
np:hasProvenance
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_provenance
;
np:hasPublicationInfo
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_assertion
a
np:Assertion
.
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_provenance
a
np:Provenance
.
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_assertion
{
miriam-gene:25793
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN65c4cbb325415600561b3af6880b30f4
sio:SIO_000628
miriam-gene:25793
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_provenance
{
dgn-np:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_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-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:NP272846.RA4Da9z5r0q0WOR-o0Y8exER4nZVSMmzTGkb06EWbJk4U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}