@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4
> .
@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:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_head
{
this:
np:hasAssertion
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_assertion
;
np:hasProvenance
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_provenance
;
np:hasPublicationInfo
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_assertion
a
np:Assertion
.
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_provenance
a
np:Provenance
.
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_assertion
{
miriam-gene:8398
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN28c49a85abf5106798e798c8466d0f8a
sio:SIO_000628
miriam-gene:8398
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_provenance
{
dgn-np:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_assertion
dcterms:description
"[Based on the clinical heterogeneity, the functional roles of PLA2G6 and the roles of PLA2G6 variants including single heterozygous mutations should be further elucidated in patients with atypical parkinsonism, dementia, or Parkinson 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:20938027
;
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:NP777802.RAA5vINIowdq5on2Tq6vZXf7cZZD0m7bTGYSHxn8kK4W4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}