@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY
> .
@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:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_head
{
this:
np:hasAssertion
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion
;
np:hasProvenance
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance
;
np:hasPublicationInfo
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion
a
np:Assertion
.
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance
a
np:Provenance
.
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion
{
miriam-gene:4642
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN99ef8963270f3a381b425bd32c36a743
sio:SIO_000628
miriam-gene:4642
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_provenance
{
dgn-np:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_assertion
dcterms:description
"[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. 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:17376794
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP85205.RA-3mGU-S6yCIpG_nZJP519wrhWJwxqGoNCd_rvc2o6SY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:26+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" .
}