@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk
> .
@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/v4.0.0/void/
> .
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_head
{
this:
np:hasAssertion
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_assertion
;
np:hasProvenance
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_provenance
;
np:hasPublicationInfo
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_assertion
a
np:Assertion
.
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_provenance
a
np:Provenance
.
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_assertion
{
miriam-gene:7353
a
ncit:C16612
.
lld:C2936346
a
ncit:C7057
.
dgn-gda:DGNe66652ff6a6d92115d52878d9b87e7bb
sio:SIO_000628
miriam-gene:7353
,
lld:C2936346
;
a
sio:SIO_001121
.
}
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_provenance
{
dgn-np:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_assertion
dcterms:description
"[UFD1L, a gene that is downregulated in dHAND-deficient mice, expressed in the mouse embryo at the branchial arch and mapped to human chromosome 22q11, has recently been strongly suspected to be responsible for the phenotypes expressed in 22q11 deletion syndromes.]. 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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP325846.RA1S3Yx1peseCHose5aWlgWeRPCPkOB1hmCfthhSRsutk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:13+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}