@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8
> .
@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:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_head
{
this:
np:hasAssertion
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_assertion
;
np:hasProvenance
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_provenance
;
np:hasPublicationInfo
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_assertion
a
np:Assertion
.
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_provenance
a
np:Provenance
.
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_assertion
{
miriam-gene:414
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGNf5f45d1670310dcaa0c3820bb93b2bd8
sio:SIO_000628
miriam-gene:414
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_provenance
{
dgn-np:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_assertion
dcterms:description
"[While it is apparent that rare variation can play an important role in the genetic architecture of autism spectrum disorders (ASDs), the contribution of common variation to the risk of developing ASD is less clear.]. 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:22843504
;
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:NP253420.RAilFl5rXtbVjMtbHP-4cJ9EFvKBVy6E4QI5H7PLIpb_8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:04+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}