@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg
> .
@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:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_head
{
this:
np:hasAssertion
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_assertion
;
np:hasProvenance
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_provenance
;
np:hasPublicationInfo
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_assertion
a
np:Assertion
.
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_provenance
a
np:Provenance
.
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0085411
a
ncit:C7057
.
dgn-gda:DGN4cc2a694010112c82383e6faec5ef6de
sio:SIO_000628
miriam-gene:7422
,
lld:C0085411
;
a
sio:SIO_001121
.
}
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_provenance
{
dgn-np:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_assertion
dcterms:description
"[Key members of the vascular endothelial growth factor (VEGF) and angiopoietin families of vascular growth factors (and their corresponding tyrosine kinase endothelial receptors) have been identified which preferentially influence lymphatic growth and, when manipulated in genetically engineered murine models, produce aberrant `lymphatic phenotypes.` Moreover, mutations in VEGF receptor and forkhead family developmental genes have now been linked and implicated in the pathogenesis of two familial lymphedema-angiodysplasia syndromes.]. 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:11596157
;
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:NP627026.RA6BLeZt9pF2-Ox2C9kr3K8U2np6IWX14cC1iPSCMimBg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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" .
}