@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM
> .
@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:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_head
{
this:
np:hasAssertion
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_assertion
;
np:hasProvenance
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_provenance
;
np:hasPublicationInfo
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_assertion
a
np:Assertion
.
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_provenance
a
np:Provenance
.
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_assertion
{
miriam-gene:4282
a
ncit:C16612
.
lld:C1533172
a
ncit:C7057
.
dgn-gda:DGNa8dab178b6de1a869c5aeb2362663541
sio:SIO_000628
miriam-gene:4282
,
lld:C1533172
;
a
sio:SIO_001121
.
}
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_provenance
{
dgn-np:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_assertion
dcterms:description
"[These results underscore the role of MIF in INS disease progression and in the response to glucocorticoid treatment and suggest that screening of MIF genotype at disease onset may identify patients requiring a more aggressive therapeutic approach.]. 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:18228042
;
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:NP173992.RAINRZDd263BCKHUNBs8rvNr9rEtMne_wXqzhp_eEt1FM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}