@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA
> .
@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:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_head
{
this:
np:hasAssertion
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion
;
np:hasProvenance
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion
a
np:Assertion
.
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance
a
np:Provenance
.
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion
{
miriam-gene:10849
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN8da43e5802a508dd44c0e9045f656764
sio:SIO_000628
miriam-gene:10849
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_provenance
{
dgn-np:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_assertion
dcterms:description
"[Using Computed Associations in Sequential Text (CAST) software to quantify the frequency of such associations in speech, we have reported more frequent normative associations in language samples from patients with schizophrenia and in individuals with schizotypal characteristics.]. 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:22819779
;
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:NP407837.RA02frgF_MI4mmstz1m8lGbsWRZLzdvuhEMQNT3PyiYFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}