@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0
> .
@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:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_head
{
this:
np:hasAssertion
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_assertion
;
np:hasProvenance
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_provenance
;
np:hasPublicationInfo
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_assertion
a
np:Assertion
.
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_provenance
a
np:Provenance
.
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_assertion
{
miriam-gene:1026
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN19029bd99fb52ac56be684e5fb5fd767
sio:SIO_000628
miriam-gene:1026
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_provenance
{
dgn-np:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_assertion
dcterms:description
"[To understand whether mutations of WAF1/Cip1 occur in cancer, we screened 53 cases of invasive breast carcinoma, 35 cases of ductal carcinoma in situ (DCIS), 53 ovarian carcinomas, and 47 endometrial carcinomas in the second exon of WAF1/Cip1 (90% of the open reading frame).]. 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:9006333
;
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:NP358603.RAoemcPuWDQwy1xvh_mTTwaqC02wE_E6tpYa_SWMlRKd0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}