@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_assertion
a
np:Assertion
.
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_provenance
a
np:Provenance
.
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3781
a
ncit:C16612
.
lld:C0006111
a
ncit:C7057
.
dgn-gda:DGNc1a21ee8b6b6c533e695d74b7e92cd51
sio:SIO_000628
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,
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;
a
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.
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dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_provenance
{
dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_assertion
dcterms:description
"[Our results suggest that genes associated with clinical neurological disease also have detectable effects on subclinical phenotypes. These hypothesis generating data illustrate the use of an unbiased approach to discover novel pathways that may be involve]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:17903297
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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 .
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dgn-np:NP156692.RAcs_sJTIMzk_hXItUv-ES7vvluVezqPR5EXpTtW8Z0fk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:09+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v3.0.0" .
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