@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU
> .
@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:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_head
{
this:
np:hasAssertion
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion
;
np:hasProvenance
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance
;
np:hasPublicationInfo
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion
a
np:Assertion
.
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance
a
np:Provenance
.
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0678236
a
ncit:C7057
.
dgn-gda:DGNc6c900e57af1924649d012743ca0c413
sio:SIO_000628
miriam-gene:3342
,
lld:C0678236
;
a
sio:SIO_001121
.
}
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_provenance
{
dgn-np:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_assertion
dcterms:description
"[METHODS Owing to the national array-CGH network funded by the French Ministry of Health, shared information about patients with rare disease helped to define critical intervals and evaluate their gene content, and finally determine the phenotypic consequences of genomic array findings.]. 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:20522426
;
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:NP527949.RAS67SI3ZS03RE1De3PJK-6dw2RdUlZCQQKd8X4HdHCVU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}