@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU
> .
@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:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_head
{
this:
np:hasAssertion
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion
;
np:hasProvenance
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance
;
np:hasPublicationInfo
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion
a
np:Assertion
.
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance
a
np:Provenance
.
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion
{
miriam-gene:5909
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGNf740e8039f12e87b50164d9a5dd1bd71
sio:SIO_000628
miriam-gene:5909
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_provenance
{
dgn-np:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_assertion
dcterms:description
"[In this study, we analyzed 197 thyroid tumor samples and showed that Rap1GAP was frequently lost or downregulated in various types of tumors, particularly in the most invasive and aggressive forms of thyroid 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:20124489
;
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:NP292389.RAAsRPQ74SDhEnPqV8h50Gq2vqMB9n98h1E1rd27r8MDU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}