@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ
> .
@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:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_head
{
this:
np:hasAssertion
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_assertion
;
np:hasProvenance
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_assertion
a
np:Assertion
.
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_provenance
a
np:Provenance
.
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN1c1eb958d23e7e335a45a85ed71cc99c
sio:SIO_000628
miriam-gene:3126
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_provenance
{
dgn-np:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_assertion
dcterms:description
"[Analyses of a 6-Mb region spanning the human leukocyte antigen (HLA) region from the HLA-DR to the HFE gene were performed in 37 families of Sardinian ancestry, all of whom had at least one autistic child, to identify genetic markers associated with autism spectrum disorders (ASD) development.]. 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:19167444
;
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:NP903678.RAAsDgGOy68Q_kpu0ppbb2MVUzgX7Bphzm3NTBQGhb4rQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}