@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc
> .
@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:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_head
{
this:
np:hasAssertion
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_assertion
;
np:hasProvenance
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_provenance
;
np:hasPublicationInfo
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_assertion
a
np:Assertion
.
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_provenance
a
np:Provenance
.
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_assertion
{
miriam-gene:2033
a
ncit:C16612
.
lld:C0041696
a
ncit:C7057
.
dgn-gda:DGNdf1fbbb14c5eb1a9b3e13191a1bae163
sio:SIO_000628
miriam-gene:2033
,
lld:C0041696
;
a
sio:SIO_001121
.
}
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_provenance
{
dgn-np:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_assertion
dcterms:description
"[Furthermore the amplitude reduction was independent of the presence or absence of symptoms because asymptomatic translocation carriers showed similar P300 amplitude reduction as was found in translocation carriers who were diagnosed with schizophrenia, bipolar disorder or unipolar depression.]. 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:15184103
;
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:NP777276.RAfppdmLTpzii2PbB2GtLsFKQb5h1U8b3z5hyCcA5i5Uc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}