@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg
> .
@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:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_head
{
this:
np:hasAssertion
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_assertion
;
np:hasProvenance
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_assertion
a
np:Assertion
.
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_provenance
a
np:Provenance
.
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_assertion
{
miriam-gene:4152
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN0d0a4b75f4c5a1999365bfc72f12c7dc
sio:SIO_000628
miriam-gene:4152
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_provenance
{
dgn-np:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_assertion
dcterms:description
"[We searched for genetic determinants of autism by (1) identifying additional chromosome copy number changes (2) Identifying common regions of hemizygosity on 18q, and (3) evaluating four regions containing candidate genes located on 18q (MBD1, TCF4, NETO1, FBXO15).]. 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:20499253
;
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:NP805636.RAXIggkBZg4eFDhu8KMdv41rGhND_TKqu_pFDkjUwezWg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}