@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak
> .
@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:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_head
{
this:
np:hasAssertion
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_assertion
;
np:hasProvenance
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_provenance
;
np:hasPublicationInfo
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_assertion
a
np:Assertion
.
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_provenance
a
np:Provenance
.
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_assertion
{
miriam-gene:2324
a
ncit:C16612
.
lld:C0238261
a
ncit:C7057
.
dgn-gda:DGN3b58349640f0c7a2b2d22275a2019517
sio:SIO_000628
miriam-gene:2324
,
lld:C0238261
;
a
sio:SIO_001121
.
}
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_provenance
{
dgn-np:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_assertion
dcterms:description
"[The prenatal nuchal lymphedema associated with this deletion syndrome my be related to the deletion of the FLT4 gene causing autosomal dominant primary lymphedema and contributes to the differential diagnosis of increased fetal nuchal translucency.]. 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:12900893
;
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:NP560345.RAXuEleM0CS3Plyf8joQbZEEGieODM-vKrP814gCF2Hak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}