@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0
> .
@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:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_head
{
this:
np:hasAssertion
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_assertion
;
np:hasProvenance
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_provenance
;
np:hasPublicationInfo
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_assertion
a
np:Assertion
.
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_provenance
a
np:Provenance
.
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_assertion
{
miriam-gene:373156
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN7a6097b973df3afd78beed5342e9b99b
sio:SIO_000628
miriam-gene:373156
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_provenance
{
dgn-np:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_assertion
dcterms:description
"[Correlations between deletions in two glutathione S-transferase (GST) genes, GSTM1 and GSTT1 and susceptibility to Alzheimer's disease (AD), motor neuron disease (MND) and Parkinson's disease (PD) have been investigated by PCR, using primers specific for both genes.]. 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:10215103
;
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:NP925504.RAR_ISEIV1MlaaDDq0-kQOpM_k8F4mGLorCETux7FabI0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
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"v2.1.0" .
}