@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg
> .
@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:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_head
{
this:
np:hasAssertion
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_assertion
;
np:hasProvenance
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_provenance
;
np:hasPublicationInfo
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_assertion
a
np:Assertion
.
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_provenance
a
np:Provenance
.
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_assertion
{
miriam-gene:7046
a
ncit:C16612
.
lld:C0039445
a
ncit:C7057
.
dgn-gda:DGNc44d18e6e7b7569adfd59de4afdf6c18
sio:SIO_000628
miriam-gene:7046
,
lld:C0039445
;
a
sio:SIO_001121
.
}
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_provenance
{
dgn-np:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_assertion
dcterms:description
"[The recent isolation and characterization of circulating endothelial cells from HHT patients has revealed a decreased endoglin expression, impaired ALK1- and ALK5-dependent TGF-beta signaling, disorganized cytoskeleton and the failure to form cord-like structures which may lead to the fragility of small vessels with bleeding characteristic of HHT vascular dysplasia or to disrupted and abnormal angiogenesis after injuries and may explain the clinical symptoms associated with this disease.]. 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:16595794
;
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:NP503430.RA9JBheIfBP8X2Flg8Wcsi15uW0PSrw6j2GcDZgR0Rqeg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}