@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s
> .
@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:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_head
{
this:
np:hasAssertion
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_assertion
;
np:hasProvenance
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_assertion
a
np:Assertion
.
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_provenance
a
np:Provenance
.
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_assertion
{
miriam-gene:100188832
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNfb02b48dc4b28f71cdd16b380959abfc
sio:SIO_000628
miriam-gene:100188832
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_provenance
{
dgn-np:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_assertion
dcterms:description
"[The region on 1q21-22 overlaps with the previously reported candidate region for infantile autism and schizophrenia, whereas the region on chromosome 7q provided evidence for linkage 58 cM distally from the previously described autism susceptibility locus (AUTS1).]. 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:12192642
;
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:NP921146.RAgtkmWObcIeL-PS971sSaOzBky8-xY6pjhohS7wvPx9s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}