@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU
> .
@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:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_head
{
this:
np:hasAssertion
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion
;
np:hasProvenance
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance
;
np:hasPublicationInfo
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion
a
np:Assertion
.
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance
a
np:Provenance
.
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGN6a828b53ab3c074b2aa339cedc173940
sio:SIO_000628
miriam-gene:7157
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_provenance
{
dgn-np:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_assertion
dcterms:description
"[This observation may correlate with the involvement of the p53 protein in spermatogenesis, with its role in aneuploidy in cancer, and with the occurrence of two cases of Turner syndrome in families with germline TP53 mutations reported in the literature.]. 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:21665182
;
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:NP590763.RAa98dAhNsrnWksuiHpIw0d0634FBKzfGM15roo13JBRU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}