@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y
> .
@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:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_head
{
this:
np:hasAssertion
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_assertion
;
np:hasProvenance
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_assertion
a
np:Assertion
.
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_provenance
a
np:Provenance
.
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN13378f460170e603b8c320fd0cf30ecf
sio:SIO_000628
miriam-gene:1312
,
lld:C0036341
;
a
sio:SIO_001122
.
}
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_provenance
{
dgn-np:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_assertion
dcterms:description
"[The COMT Val158Met polymorphism did not appear to significantly affect susceptibility, symptomatology, global cognitive function and prognosis in Chinese patients with schizophrenia, but the possible association with AOO merits further investigation.]. 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:15118357
;
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:NP442133.RAWp6abBxps68drnbbFHAsyRrpUF4LlSeGTwauEDG2T9Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:05+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
<
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" .
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pav:version
"v4.0.0" .
}