@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0
> .
@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:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_head
{
this:
np:hasAssertion
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_assertion
;
np:hasProvenance
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_provenance
;
np:hasPublicationInfo
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_assertion
a
np:Assertion
.
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_provenance
a
np:Provenance
.
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_assertion
{
miriam-gene:259232
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN7cd16141eaad778001d3aef4c9c40cab
sio:SIO_000628
miriam-gene:259232
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_provenance
{
dgn-np:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_assertion
dcterms:description
"[Although NALCN variants have been conflictingly reported to be in linkage disequilibrium with schizophrenia and bipolar disorder, to our knowledge, no mutations have been reported to date for any inherited disorders.]. 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:24075186
;
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:NP539885.RASjlw69eqVHZZXLWFH9zn4Ucyd1xaO7STU9ybxN4NVL0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}