@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI
> .
@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:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_head
{
this:
np:hasAssertion
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_assertion
;
np:hasProvenance
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_provenance
;
np:hasPublicationInfo
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_assertion
a
np:Assertion
.
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_provenance
a
np:Provenance
.
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN64b16e471730669ef3dfa8716122f464
sio:SIO_000628
miriam-gene:3358
,
lld:C0004936
;
a
sio:SIO_001121
.
}
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_provenance
{
dgn-np:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_assertion
dcterms:description
"[Studies in humans have reported abnormalities in patterns of HTR2C editing in psychiatric disorders, and studies in rodents show altered patterns of editing in response to drug treatments and stressful situations.]. 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:17307311
;
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:NP884369.RALjA0OmIcJNX5nNBeLSdigTpo_CN4MNKNSRgGjfslBHI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}