@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo
> .
@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:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_head
{
this:
np:hasAssertion
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_assertion
;
np:hasProvenance
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_provenance
;
np:hasPublicationInfo
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_assertion
a
np:Assertion
.
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_provenance
a
np:Provenance
.
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_assertion
{
miriam-gene:5071
a
ncit:C16612
.
lld:C0752100
a
ncit:C7057
.
dgn-gda:DGN119af0b308c3a379abe4d9121a6511ac
sio:SIO_000628
miriam-gene:5071
,
lld:C0752100
;
a
sio:SIO_001121
.
}
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_provenance
{
dgn-np:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_assertion
dcterms:description
"[A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.]. 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:10072423
;
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:NP247401.RAugHaxbjSXWmrs0A5kcrMaGlfIoja2jLteEboEZbuDFo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:38+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" .
}