@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s
> .
@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:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_head
{
this:
np:hasAssertion
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_assertion
;
np:hasProvenance
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_assertion
a
np:Assertion
.
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_provenance
a
np:Provenance
.
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0349204
a
ncit:C7057
.
dgn-gda:DGN5ff180bb4e78697c0458cbf6a8a65fb8
sio:SIO_000628
miriam-gene:2837
,
lld:C0349204
;
a
sio:SIO_001121
.
}
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_provenance
{
dgn-np:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_assertion
dcterms:description
"[We performed Sanger sequencing of all 28 exons in ERBB4, as well as part of the promoter and part of the 3'UTR sequence, hypothesizing that rare deleterious variants would be found in 188 cases with mood-incongruent psychosis from the GAIN BP study.]. 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:21637803
;
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:NP869038.RA2GcHKx47lZxfVKj13wqGcBO1322FD2xkqxg6rfK7Z1s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:51+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" .
}