@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw
> .
@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:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_head
{
this:
np:hasAssertion
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion
;
np:hasProvenance
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance
;
np:hasPublicationInfo
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion
a
np:Assertion
.
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance
a
np:Provenance
.
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion
{
miriam-gene:4810
a
ncit:C16612
.
lld:C0424605
a
ncit:C7057
.
dgn-gda:DGN86bc93acaa9b840063455f8f2041d8e3
sio:SIO_000628
miriam-gene:4810
,
lld:C0424605
;
a
sio:SIO_001121
.
}
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_provenance
{
dgn-np:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_assertion
dcterms:description
"[Audit of findings from application of array CGH for patients referred for developmental delay, behavioural abnormalities and birth defects in 4805 patients referred to Guy's and St Thomas' NHS Foundation Trust for cytogenetic investigation from South East London, Kent and East Sussex and other genetic centres across the UK.]. 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:21429933
;
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:NP882344.RAygq76fr6AYC-LDEGBteiGxF0CbcdF3xWodyBI2vzYgw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}