@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE
> .
@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 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:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_head
{
this:
np:hasAssertion
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_assertion
;
np:hasProvenance
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_provenance
;
np:hasPublicationInfo
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_assertion
a
np:Assertion
.
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_provenance
a
np:Provenance
.
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_assertion
{
miriam-gene:154
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNaff5615add31f9baf48dc4b5099a061b
sio:SIO_000628
miriam-gene:154
,
lld:C0026769
;
a
sio:SIO_001122
.
}
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_provenance
{
dgn-np:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_assertion
dct:description
"[Together, our findings suggest that the presence of beta2AR gene polymorphisms may be inconclusive in the susceptibility to MS or in the clinical characteristics of Japanese patients with MS and, therefore, need further studies.]. 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:12474986
;
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:NP49058.RAiFxKZMJ21YaVX3amSeHEmTg8yE859LiVpt4PNtnZ3mE130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}