@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw
> .
@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:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_head
{
this:
np:hasAssertion
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_assertion
;
np:hasProvenance
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_provenance
;
np:hasPublicationInfo
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_assertion
a
np:Assertion
.
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_provenance
a
np:Provenance
.
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_assertion
{
miriam-gene:7314
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN3c4bda5cbb1462edc9c70936266c2cbf
sio:SIO_000628
miriam-gene:7314
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_provenance
{
dgn-np:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_assertion
dcterms:description
"[A case study using Parkinson disease (PD) has identified four candidate genes (UBB, SEPT5, GPR37 and TH) that ranked higher than our adaptive threshold, all of which are involved in the PD pathway.]. 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:21731658
;
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:NP537691.RAmhE_i1xLpfcUAB2FWPvCdOjh_lobWaJPzLM_7yH3pHw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}