@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE
> .
@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:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_head
{
this:
np:hasAssertion
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_assertion
;
np:hasProvenance
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_assertion
a
np:Assertion
.
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_provenance
a
np:Provenance
.
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_assertion
{
miriam-gene:7405
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN4eff3608efa6991fe3d0dfe4f22f7210
sio:SIO_000628
miriam-gene:7405
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_provenance
{
dgn-np:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_assertion
dcterms:description
"[We point out common themes and features, that allow to speculate on the possible role of p63 downstream events and their potential exploitation in future attempts to correct the congenital defect in preclinical studies.]. 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:21716671
;
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:NP906008.RA1vwbybs946c1mwq2xjUk6xG0_SyqXckN1JFf5p7BZhE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:34+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" .
}