@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU
> .
@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:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_head
{
this:
np:hasAssertion
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_assertion
;
np:hasProvenance
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_provenance
;
np:hasPublicationInfo
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_assertion
a
np:Assertion
.
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_provenance
a
np:Provenance
.
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_assertion
{
miriam-gene:23209
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNc09c59332f9d27cb5aa7286bfa29aed4
sio:SIO_000628
miriam-gene:23209
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_provenance
{
dgn-np:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_assertion
dcterms:description
"[In addition, initial reports suggested that a rare variant in exon 11 (L309M) is involved in the etiology of schizophrenia, but recent studies have brought forward compelling arguments that genetic variants of MLC1 are not associated with schizophrenia.]. 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:12477442
;
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:NP848496.RAXdcLQ9eQyafkaQ81j4o5QniQBMZAP52N2Y42OAzdryU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}