@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM
> .
@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:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_head
{
this:
np:hasAssertion
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_assertion
;
np:hasProvenance
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_provenance
;
np:hasPublicationInfo
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_assertion
a
np:Assertion
.
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_provenance
a
np:Provenance
.
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_assertion
{
miriam-gene:1270
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN96ded7b5685fb1f7d467fd0d822bf001
sio:SIO_000628
miriam-gene:1270
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_provenance
{
dgn-np:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_assertion
dcterms:description
"[It is concluded that the CNTF null mutation may be relevant to the aetiopathogenesis of schizophrenia in some patients, but further work is required to identify specifically the patient group for which it is important.]. 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:8856688
;
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:NP161577.RAN5bNmCPMEpuZPZfR5p7zJkxA4MUs1vacSLc2d1zsWoM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}