@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8
> .
@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:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_head
{
this:
np:hasAssertion
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_assertion
;
np:hasProvenance
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_assertion
a
np:Assertion
.
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_provenance
a
np:Provenance
.
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0035258
a
ncit:C7057
.
dgn-gda:DGNaabc30f546e4de39f3dcc193d2017e1f
sio:SIO_000628
miriam-gene:1312
,
lld:C0035258
;
a
sio:SIO_001122
.
}
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_provenance
{
dgn-np:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_assertion
dcterms:description
"[The data revealed no significant differences in the distribution of the COMT val(158)met polymorphism in RLS patients compared with the control group, also when the heterozygous and the homozygous group containing the (158)met allele were combined.]. 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:20184941
;
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:NP89353.RAeLp5WrvXgDtwUNQnEiDajaVLQjBdpWRJ6tNYxr4QFV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}