@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo
> .
@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:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_head
{
this:
np:hasAssertion
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_assertion
;
np:hasProvenance
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_provenance
;
np:hasPublicationInfo
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_assertion
a
np:Assertion
.
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_provenance
a
np:Provenance
.
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0428791
a
ncit:C7057
.
dgn-gda:DGNb5bb37742c360e04e3860c4022ebb89d
sio:SIO_000628
miriam-gene:7422
,
lld:C0428791
;
a
sio:SIO_001121
.
}
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_provenance
{
dgn-np:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_assertion
dcterms:description
"[Recently, various human studies have revealed a high coincidence of VEGF and NOTCH polymorphisms with cardiovascular outflow tract anomalies, such as bicuspid aortic valves and Tetralogy of Fallot, next to predisposition for cardiovascular pathologies, including atherosclerosis and aortic valve calcification.]. 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:22683047
;
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:NP772037.RARkqtJ2kGP4mdYEvRYyvtlzS09oqkmAQYHoHTe9iKdTo130_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" .
}