@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco
> .
@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:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_head
{
this:
np:hasAssertion
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_assertion
;
np:hasProvenance
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_provenance
;
np:hasPublicationInfo
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_assertion
a
np:Assertion
.
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_provenance
a
np:Provenance
.
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_assertion
{
miriam-gene:773
a
ncit:C16612
.
lld:C0014553
a
ncit:C7057
.
dgn-gda:DGN69960bcc47e7837f4668a6e8d5547271
sio:SIO_000628
miriam-gene:773
,
lld:C0014553
;
a
sio:SIO_001121
.
}
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_provenance
{
dgn-np:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_assertion
dcterms:description
"[Cav2.1 (P/Q-type) calcium channels control synaptic transmission at presynaptic nerve terminals, and mutations in the gene encoding the Cav2.1 alpha1 subunit (CACNA1A) have been linked to absence seizures in both humans and rodents.]. 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:20091047
;
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:NP300248.RANRN6M8vCY5PXldZtknQwLiZv9KvdD8RBqa0xz-4egco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}