@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo
> .
@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:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_head
{
this:
np:hasAssertion
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_assertion
;
np:hasProvenance
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_provenance
;
np:hasPublicationInfo
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_assertion
a
np:Assertion
.
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_provenance
a
np:Provenance
.
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0040822
a
ncit:C7057
.
dgn-gda:DGNa36749c86de886542f5abb6797815278
sio:SIO_000628
miriam-gene:120892
,
lld:C0040822
;
a
sio:SIO_001121
.
}
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_provenance
{
dgn-np:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_assertion
dcterms:description
"[LRRK2 mutation carriers were previously reported to manifest the tremor dominant motor phenotype, which has been associated with slower motor progression and less cognitive impairment compared with the postural instability and gait difficulty (PIGD) phenotype.]. 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:20008657
;
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:NP696019.RAFYDcSBkfm-op71m0aN3UFv4TV72iMNIUjhO_2_ktONo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}