@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg
> .
@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:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_head
{
this:
np:hasAssertion
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion
;
np:hasProvenance
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion
a
np:Assertion
.
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance
a
np:Provenance
.
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion
{
miriam-gene:127
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN57fee924cf4d3fe002f90a9d6e8ab253
sio:SIO_000628
miriam-gene:127
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_provenance
{
dgn-np:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_assertion
dcterms:description
"[an association between a certain ADH4 (formerly known as ADH7 in humans) allele and PD. This suggests a role for genetic variations of ADH4 as risk factors for the development of PD. Our data also show that the observed polymorphisms alone are not sufficient to cause symptoms. Further genetic and/or environmental factors have to be involved.]. 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:11009184
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP49195.RATlxJx4Bkx_48309z6mfZ2d3D2xZq8AHqbWFhxwAaoWg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}