@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_head
{
this:
np:hasAssertion
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_assertion
;
np:hasProvenance
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_provenance
;
np:hasPublicationInfo
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_assertion
a
np:Assertion
.
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_provenance
a
np:Provenance
.
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_assertion
{
miriam-gene:952
a
ncit:C16612
.
lld:C0018817
a
ncit:C7057
.
dgn-gda:DGN4fd1b03f233aee0bfe5f1ea4994c57d1
sio:SIO_000628
miriam-gene:952
,
lld:C0018817
;
a
sio:SIO_001121
.
}
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_provenance
{
dgn-np:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_assertion
dcterms:description
"[While a number of studies have implicated rare chromosomal deletions and duplications in helping determine genetic risk for autism, there are to our knowledge no reports describing rearrangements involving CD38 or deletions in patients with ASD.]. 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:24634087
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP294051.RAPCty5d0BAceQkYnHxkhn-o3RTu7Zfy5W-ehSmKzvZo0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:28+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}