@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI
> .
@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/v3.0.0/void/
> .
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_head
{
this:
np:hasAssertion
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_assertion
;
np:hasProvenance
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_assertion
a
np:Assertion
.
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_provenance
a
np:Provenance
.
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGN01a4b431c9db7e435852d9a3eae52d8e
sio:SIO_000628
miriam-gene:7422
,
lld:C0152021
;
a
sio:SIO_001122
.
}
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_provenance
{
dgn-np:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP771354.RAbmSBPe7dA46tBf8AG0MKR3_y_tYlWS3yafDkTpTvfRI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:26+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}