@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk
> .
@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:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_head
{
this:
np:hasAssertion
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_assertion
;
np:hasProvenance
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_assertion
a
np:Assertion
.
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_provenance
a
np:Provenance
.
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_assertion
{
miriam-gene:55349
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN3dfd0e9dd9dee7d7ec3e723042591b5f
sio:SIO_000628
miriam-gene:55349
,
lld:C0018799
;
a
sio:SIO_001122
.
}
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_provenance
{
dgn-np:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_assertion
dcterms:description
"[Depression was more severe (Hamilton score) if it was caused by manifestation or exacerbation of CHD (nosogenic factor) and in the presence of the painful syndrome caused by the cardiac disease, high personal anxiety, and presence of allele G polymorphism - 1438A/G in the genotype.]. 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:24770757
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1177095.RAOCRw_xptdJWgE-ie3Pz75wNHMYDEjKfDodgETofGesk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:39+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}