@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4
> .
@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:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_head
{
this:
np:hasAssertion
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion
;
np:hasProvenance
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance
;
np:hasPublicationInfo
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion
a
np:Assertion
.
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance
a
np:Provenance
.
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0018923
a
ncit:C7057
.
dgn-gda:DGNd9fe95714653859ffbd2abb212cb9dae
sio:SIO_000628
miriam-gene:4193
,
lld:C0018923
;
a
sio:SIO_001121
.
}
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_provenance
{
dgn-np:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_assertion
dcterms:description
"[Although p14 inactivation or overexpression of the human murine double minute homolog (HDM2) were frequent in LMS and UPS and could substitute for TP53 mutation or deletion, such alterations were rare in angiosarcomas.]. 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:22648906
;
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:NP986137.RAp_SlWB3Hpt92onEtgzbJ_LFn3jwrVApgRVD3fEEA0a4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:12+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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" .
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pav:version
"v4.0.0" .
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