@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA
> .
@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:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_head
{
this:
np:hasAssertion
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_assertion
;
np:hasProvenance
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_provenance
;
np:hasPublicationInfo
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_assertion
a
np:Assertion
.
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_provenance
a
np:Provenance
.
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_assertion
{
miriam-gene:7329
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN686d1933781ae62104a8da0abd58fc94
sio:SIO_000628
miriam-gene:7329
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_provenance
{
dgn-np:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_assertion
dcterms:description
"[This loss of p18(Ink4c) expression correlated with higher proliferation rates as well as with larger MTCs, indicating that loss of p18 in combination with oncogenic RET not only increases the risk for MTC development but also enhances MTC progression.]. 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:18316595
;
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:NP191559.RA1quQCH_qNbfMMTCz1h6xCq7qlCEVPvOv5vbNAtJHbEA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}