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http://rdf.disgenet.org/nanopublications.trig#NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw
> .
@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#
> .
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{
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_provenance
a
np:Provenance
.
dgn-np:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8896
a
ncit:C16612
.
lld:C0024307
a
ncit:C7057
.
dgn-gda:DGNe0040763ebc04548830e2b8a27d152ed
sio:SIO_000628
miriam-gene:8896
,
lld:C0024307
;
a
sio:SIO_001121
.
}
dgn-np:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_provenance
{
dgn-np:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_assertion
dcterms:description
"[We used high resolution quantitative trait loci (QTL) analysis in the 10th generation (G10) of an advanced intercross line (AIL) to resolve Eae23 into two QTLs that independently regulate EAE, namely Eae23a and Eae23b.]. 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:20856809
;
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:NP721459.RAcoSaWCs62f_0tA7TFcNraxEgWwzTpJEo0BjKuKZUdkw130_publicationInfo
{
this:
dcterms:created
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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
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> , <
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> , <
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> , <
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
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"v2.1.0" .
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