@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y
> .
@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:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_head
{
this:
np:hasAssertion
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_assertion
;
np:hasProvenance
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_assertion
a
np:Assertion
.
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_provenance
a
np:Provenance
.
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_assertion
{
miriam-gene:30816
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN42faaba0b550bc7ac469a26236549602
sio:SIO_000628
miriam-gene:30816
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_provenance
{
dgn-np:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_assertion
dcterms:description
"[Although genetic variations in several genes encoding for synaptic adhesion proteins have been found to be associated with autism spectrum disorders, one of the most consistently replicated genes has been CNTNAP2, encoding for contactin-associated protein-like 2 (CASPR2), a multidomain transmembrane protein of the neurexin superfamily.]. 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:22872700
;
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:NP816990.RAvejY3ZwUuAPobXKwWuBk51tIrdJpdn7v6MU_DYEGT6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}