@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw
> .
@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/v3.0.0/void/
> .
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_head
{
this:
np:hasAssertion
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion
;
np:hasProvenance
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion
a
np:Assertion
.
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance
a
np:Provenance
.
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion
{
miriam-gene:84894
a
ncit:C16612
.
lld:C0270736
a
ncit:C7057
.
dgn-gda:DGN815a75c015c688502d7d1efefefc1b24
sio:SIO_000628
miriam-gene:84894
,
lld:C0270736
;
a
sio:SIO_001121
.
}
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_provenance
{
dgn-np:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_assertion
dcterms:description
"[In addition, we also investigated the variant in patients with Parkinson disease (PD) because the GWAS LINGO1 variant has been implicated in both ET and PD and etiologic links between the conditions have been suggested.(6.]. 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:23596072
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP958528.RAp9GdkzZ8aK-Ume1EesblC2wRocptORqvP7oOwgvJnFw130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:25+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}