@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_assertion
;
np:hasProvenance
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_assertion
a
np:Assertion
.
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_provenance
a
np:Provenance
.
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_assertion
{
miriam-gene:83478
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNa7db51bb57d48c37187cbb75877da1c1
sio:SIO_000628
miriam-gene:83478
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_provenance
{
dgn-np:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_assertion
dcterms:description
"[Because p63 and p73 are rarely mutated in human cancer, understanding the signaling pathways that activate p63 and p73 will not only shed light on the developmental processes regulated by p63 and p73 but may also yield insight into ways to harness p63 and p73 activity for cancer therapy.]. 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:16738062
;
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:NP194792.RAwuz3-KD0yDTVJhij8p0S5CJfv1CmrEKG_a7ir0awdiM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}