@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s
> .
@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/
> .
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_head
{
this:
np:hasAssertion
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_assertion
;
np:hasProvenance
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_assertion
a
np:Assertion
.
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_provenance
a
np:Provenance
.
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_assertion
{
miriam-gene:84692
a
ncit:C16612
.
lld:C0700327
a
ncit:C7057
.
dgn-gda:DGNe56f22fd49f5d145a0f8467037ef9469
sio:SIO_000628
miriam-gene:84692
,
lld:C0700327
;
a
sio:SIO_001122
.
}
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_provenance
{
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_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 .
}
dgn-np:NP156759.RANrh1LCWJfRFV36xZtGcyq1V1SxjEiCfYP2uJ7l7XZ5s130_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
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}