@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY
> .
@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:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_head
{
this:
np:hasAssertion
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_assertion
;
np:hasProvenance
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_assertion
a
np:Assertion
.
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_provenance
a
np:Provenance
.
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN6cd6486210a8f8b49318d34991c659bb
sio:SIO_000628
miriam-gene:7157
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_provenance
{
dgn-np:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_assertion
dcterms:description
"[Whereas in sporadic human malignancies mutations of the TP53 tumor-suppressor gene occur in cancers of almost every organ and histologic subtype, patients with an inborn TP53 defect are at high risk to develop, in particular, soft tissue and bone sarcomas, brain tumors, leukaemias, adrenocortical tumors, and breast cancer.]. 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:11920788
;
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:NP349998.RAbtm6eoQqVGYcsomCkqKe-Z-_FhTtub4TOc2fSlleoGY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:24+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" .
}