@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_head
{
this:
np:hasAssertion
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion
;
np:hasProvenance
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance
;
np:hasPublicationInfo
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion
a
np:Assertion
.
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance
a
np:Provenance
.
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion
{
miriam-gene:2324
a
ncit:C16612
.
lld:C1704423
a
ncit:C7057
.
dgn-gda:DGN9d9322dd5062565d086b088a8e4f7bce
sio:SIO_000628
miriam-gene:2324
,
lld:C1704423
;
a
sio:SIO_001121
.
}
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_provenance
{
dgn-np:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_assertion
dcterms:description
"[The clinical presentation, similar to Milroy disease, indicates an overlapping of the external phenotype of both diseases, suggesting that genetic analysis of VEGFC would be useful in diagnosing patients that present with Milroy features but have no mutation in VEGFR-3.]. 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:24744435
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP408551.RAx0PbNhX9bgPe4gTyDT0TFUDJg25rLvIhhsHMpVPdoPk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:37+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}