@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg
> .
@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:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_head
{
this:
np:hasAssertion
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_assertion
;
np:hasProvenance
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_provenance
;
np:hasPublicationInfo
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_assertion
a
np:Assertion
.
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_provenance
a
np:Provenance
.
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0270736
a
ncit:C7057
.
dgn-gda:DGN75c7ddc63c6566d9050643fcfb50f234
sio:SIO_000628
miriam-gene:120892
,
lld:C0270736
;
a
sio:SIO_001121
.
}
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_provenance
{
dgn-np:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_assertion
dcterms:description
"[To evaluate the frequency of the LRRK2 P755L variant in North American Caucasian patients with PD, we screened 426 PD patients and 37 additional patients with the combination of PD and essential tremor (ET) from our Parkinson Disease Center and Movement Clinic at Baylor College of Medicine.]. 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:17482357
;
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:NP923635.RAyipvtK1ndjhMi9tBwLJSatZmWkjhHD0AuHdErZyoyfg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}