@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM
> .
@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:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_assertion
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np:hasProvenance
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_provenance
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np:hasPublicationInfo
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_assertion
a
np:Assertion
.
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_provenance
a
np:Provenance
.
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0334424
a
ncit:C7057
.
dgn-gda:DGNd6dfd4db4bc2a336639c0a56805af945
sio:SIO_000628
miriam-gene:7157
,
lld:C0334424
;
a
sio:SIO_001121
.
}
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_provenance
{
dgn-np:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_assertion
dcterms:description
"[Our data show that hPTTG1 is frequently overexpressed in nodular melanoma, and suggest that hPTTG1 may act as an oncogene in the vertical growth phase, either by inhibiting anaphase, thereby causing aneuploidy and genomic instability, or by modulating the function of p53, thereby impairing apoptosis.]. 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:16799481
;
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:NP577671.RA0mFvzTJAoxAMRd9EuO1J8fvruyqdtogAWMz5AxNnJNM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+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
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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dgn-void:disgenetrdf
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