@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc
> .
@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:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_head
{
this:
np:hasAssertion
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_assertion
;
np:hasProvenance
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_provenance
;
np:hasPublicationInfo
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_assertion
a
np:Assertion
.
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_provenance
a
np:Provenance
.
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_assertion
{
miriam-gene:23630
a
ncit:C16612
.
lld:C0018798
a
ncit:C7057
.
dgn-gda:DGNe6f2088922cc6b80febd6f9b1f585eae
sio:SIO_000628
miriam-gene:23630
,
lld:C0018798
;
a
sio:SIO_001121
.
}
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_provenance
{
dgn-np:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_assertion
dcterms:description
"[The specific distribution in adult tissues, the putative channel function, and the expression pp6tern in the developing mouse embryo suggest that KCNE1L could be involved in the development of the cardiac abnormalities as well as of some neurological signs observed in patients with AMME contiguous gene syndrome.]. 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:10493825
;
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:NP753002.RAX2_EZXTpRLB3btgrpX37110U2bFKQRLJovRkLHLzNCc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}