@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s
> .
@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:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_assertion
;
np:hasProvenance
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_provenance
;
np:hasPublicationInfo
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_assertion
a
np:Assertion
.
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_provenance
a
np:Provenance
.
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0014084
a
ncit:C7057
.
dgn-gda:DGN427ca358b20e6e262d8c810ed75bf794
sio:SIO_000628
miriam-gene:7157
,
lld:C0014084
;
a
sio:SIO_001121
.
}
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_provenance
{
dgn-np:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_assertion
dcterms:description
"[It is hypothesized that inactivation of putative tumor suppressor genes at 9p21 and 13q14, and overexpression of p53, identified in the chondrosarcoma and its metastases, but absent in enchondroma, may be related to sarcomatous transformation in Ollier's disease.]. 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:11070122
;
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:NP408062.RA_A_HMk426ycG4oDDcKOJNxRL99kUhwjgExKncfqVO0s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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
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"v2.1.0" .
}