@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY
> .
@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:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_head
{
this:
np:hasAssertion
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion
;
np:hasProvenance
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance
;
np:hasPublicationInfo
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion
a
np:Assertion
.
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance
a
np:Provenance
.
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion
{
miriam-gene:11146
a
ncit:C16612
.
lld:C1841984
a
ncit:C7057
.
dgn-gda:DGN21bc4f375f54b313cc9b46e3f06e24c8
sio:SIO_000628
miriam-gene:11146
,
lld:C1841984
;
a
sio:SIO_001121
.
}
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_provenance
{
dgn-np:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_assertion
dcterms:description
"[The common mesenchymal origin of GVM and lymphatic vessels as well as the glomulin expression in vascular smooth muscle cells in utero could help explain this unusual prenatal complication of glomuvenous malformations.]. 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:21510024
;
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:NP444583.RAr0qLQFDaFknzHoCTOSTY9qVF7oV3EpLyQdIEVz_XSnY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}