@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo
> .
@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:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_head
{
this:
np:hasAssertion
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion
;
np:hasProvenance
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance
;
np:hasPublicationInfo
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion
a
np:Assertion
.
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance
a
np:Provenance
.
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion
{
miriam-gene:5921
a
ncit:C16612
.
lld:C0205788
a
ncit:C7057
.
dgn-gda:DGN49c1df6bcf9a8b3b176bf9cf9cf80b2d
sio:SIO_000628
miriam-gene:5921
,
lld:C0205788
;
a
sio:SIO_001121
.
}
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_provenance
{
dgn-np:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_assertion
dcterms:description
"[In addition to the reported venous malformation, such mutations were identified in some other subtypes of vascular anomalies, including vascular tumors (infantile hemangioma, pyogenic granuloma, and epithelioid hemangioma) and vascular malformations (capillary malformation, arteriovenous malformation, capillary lymphatic malformation, and capillary arteriovenous malformation).]. 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:21962923
;
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:NP426115.RAKr8pxg02Fz-EZlLPUOsGN3fdXbTV9kYslPG7pXLUUbo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}