@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_head
{
this:
np:hasAssertion
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_assertion
;
np:hasProvenance
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_assertion
a
np:Assertion
.
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_provenance
a
np:Provenance
.
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_assertion
{
miriam-gene:858
a
ncit:C16612
.
lld:C0936250
a
ncit:C7057
.
dgn-gda:DGN0a2e83146a0cb086871a7a86f6f993ed
sio:SIO_000628
miriam-gene:858
,
lld:C0936250
;
a
sio:SIO_001121
.
}
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_provenance
{
dgn-np:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_assertion
dcterms:description
"[To investigate genetic determinants of novel clinical phenotypes of CVA6, we genetically characterized and analysed CVA6 variants associated with eczema herpeticum in Edinburgh in 2014 and those with aHFMD in CAV isolates collected from 2008.]. 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:25614593
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1257889.RAoTLjNtGR-REOh60SS32HloIT334TYfUmQ2sm98mkn1o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}