@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo
> .
@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:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_head
{
this:
np:hasAssertion
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_assertion
;
np:hasProvenance
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_provenance
;
np:hasPublicationInfo
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_assertion
a
np:Assertion
.
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_provenance
a
np:Provenance
.
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_assertion
{
miriam-gene:1125
a
ncit:C16612
.
lld:C0033975
a
ncit:C7057
.
dgn-gda:DGNd327d8139388bcbcbe6339065ccf966c
sio:SIO_000628
miriam-gene:1125
,
lld:C0033975
;
a
sio:SIO_001121
.
}
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_provenance
{
dgn-np:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_assertion
dcterms:description
"[Risk for psychosis can be assessed on the basis of genetic risk, referred to in the literature as family high risk (FHR) or through the presence of clinical high risk symptoms (CHR).]. 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:23611242
;
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:NP734093.RAAocfaIbSSwej4D4Q5nqgCi9i1Z2xeATi9B6q3xrDQTo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}