@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s
> .
@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:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_head
{
this:
np:hasAssertion
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion
;
np:hasProvenance
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance
;
np:hasPublicationInfo
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion
a
np:Assertion
.
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance
a
np:Provenance
.
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion
{
miriam-gene:2324
a
ncit:C16612
.
lld:C0020305
a
ncit:C7057
.
dgn-gda:DGNc346c4fc2e3fbd6efaf4855fdb353c33
sio:SIO_000628
miriam-gene:2324
,
lld:C0020305
;
a
sio:SIO_001121
.
}
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_provenance
{
dgn-np:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_assertion
dcterms:description
"[Because VEGFR3 mutation can cause generalized lymphatic dysfunction and can thus result in hydrops fetalis, VEGFR3 screening should be added to the investigation of cases of hydrops fetalis of an unknown etiology.]. 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:16965327
;
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:NP821574.RAdg_l2qIXiKZchNFWgd39zNy__NoC0jpSfDlU27c-S2s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}