@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c
> .
@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:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_head
{
this:
np:hasAssertion
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_assertion
;
np:hasProvenance
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_provenance
;
np:hasPublicationInfo
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_assertion
a
np:Assertion
.
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_provenance
a
np:Provenance
.
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_assertion
{
miriam-gene:10168
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGN8220a733110c9429692c0e0c7dab75a0
sio:SIO_000628
miriam-gene:10168
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_provenance
{
dgn-np:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_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:NP322215.RAl9mCnMnK_sM2y7xJ1edG7SueiDjFVwgx72fPuEy-21c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:08+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" .
}