@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q
> .
@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:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_head
{
this:
np:hasAssertion
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_assertion
;
np:hasProvenance
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_assertion
a
np:Assertion
.
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_provenance
a
np:Provenance
.
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGNec082686f7e316bffeb676575421d2b5
sio:SIO_000628
miriam-gene:7422
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_provenance
{
dgn-np:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_assertion
dcterms:description
"[Our results provide further evidence of the incomplete penetrance of the cardiovascular phenotype of microdeletion 22ql 1, but do not support association between VEGFA promoter polymorphisms and the presence of congenital heart disease in Chilean patients with this 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:20140301
;
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:NP291419.RA6X3bpvJEJ3ZptXY9ZsnFDr5fdMYVcXnhgI7Z9DO_N6Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}