@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg
> .
@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:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_head
{
this:
np:hasAssertion
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_assertion
;
np:hasProvenance
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_provenance
;
np:hasPublicationInfo
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_assertion
a
np:Assertion
.
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_provenance
a
np:Provenance
.
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_assertion
{
miriam-gene:3912
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNb7a6d404944550e1208086b3d260b0c9
sio:SIO_000628
miriam-gene:3912
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_provenance
{
dgn-np:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_assertion
dcterms:description
"[Four candidate genes (NRCAM, LRRN3, KIAA0716, and LAMB1) in this region were chosen for examination based on their proximity to the marker most consistently cosegregating with autism in these families (D7S1817), their tissue expression patterns, and likely biological relevance to autism.]. 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:15128462
;
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:NP501780.RAdSATn5G5YrBMpHbUqkOzo01U9u1DQej3fZCNbq4zXRg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}