@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0
> .
@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:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_head
{
this:
np:hasAssertion
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion
;
np:hasProvenance
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion
a
np:Assertion
.
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance
a
np:Provenance
.
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion
{
miriam-gene:8626
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN02e415669a3add1cda48a09dceabf398
sio:SIO_000628
miriam-gene:8626
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_provenance
{
dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_assertion
dcterms:description
"[As mutants of p63 in humans exhibit phenotypes that cause several autosomal dominantly inherited syndromes leading to developmental malformations, we tested the transcriptional response of TAp63γ mutants derived from the EEC, SHFM and ADULT 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:20543567
;
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 .
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dgn-np:NP670547.RAAEMq6Ip4fvBRHtt4VMMxfiIog93Z79c8zJgTTafKLr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}