@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg
> .
@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:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_head
{
this:
np:hasAssertion
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_assertion
;
np:hasProvenance
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_provenance
;
np:hasPublicationInfo
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_assertion
a
np:Assertion
.
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_provenance
a
np:Provenance
.
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_assertion
{
miriam-gene:7353
a
ncit:C16612
.
lld:C0039685
a
ncit:C7057
.
dgn-gda:DGNf30f948544b9a9c1e55d58525b8c9942
sio:SIO_000628
miriam-gene:7353
,
lld:C0039685
;
a
sio:SIO_001121
.
}
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_provenance
{
dgn-np:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_assertion
dcterms:description
"[Our data suggest that, although the UFD1L gene is mapped to 22q11 and is expressed during early murine development at both cardiac and cranial neural crests, it is not responsible for the majority of tetralogy of Fallot cases in humans.]. 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:11485030
;
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:NP587342.RA_Y0k664C-Z9ymQPnvfUHCr5iEQk8BdmbX-PwGp32Vsg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}