@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0
> .
@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:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_head
{
this:
np:hasAssertion
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_assertion
;
np:hasProvenance
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_provenance
;
np:hasPublicationInfo
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_assertion
a
np:Assertion
.
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_provenance
a
np:Provenance
.
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0008479
a
ncit:C7057
.
dgn-gda:DGN0a4a513bf368713d3853882792129e70
sio:SIO_000628
miriam-gene:5728
,
lld:C0008479
;
a
sio:SIO_001121
.
}
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_provenance
{
dgn-np:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_assertion
dcterms:description
"[Mutations in the exons of p16, alterations of the putative tumor suppressor gene MMAC1/PTEN on chromosome 10q, or an amplification of the cyclin D1 gene (CCND1) on 11q13, which were found to be changed in other studies of chondrosarcomas, could not be demonstrated here.]. 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:11859213
;
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:NP775591.RAp9_2EeiNYOG3rPS7eXS09ZGDyZt_M9aJnAFLAlS8qN0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}