@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg
> .
@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/v4.0.0/void/
> .
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_head
{
this:
np:hasAssertion
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_assertion
;
np:hasProvenance
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_provenance
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np:hasPublicationInfo
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_assertion
a
np:Assertion
.
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_provenance
a
np:Provenance
.
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:10413
a
ncit:C16612
.
lld:C0006111
a
ncit:C7057
.
dgn-gda:DGNee1eef4dea1d6ab8a5f41a958c821f98
sio:SIO_000628
miriam-gene:10413
,
lld:C0006111
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.
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dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_provenance
{
dgn-np:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_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
;
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:NP112735.RAQroBh2MJIZEooPLiujGpYk4JQDlN8bBABSfHnwPc7Xg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:38+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
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;
pav:authoredBy
<
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> , <
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> , <
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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