@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U
> .
@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:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_head
{
this:
np:hasAssertion
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_assertion
;
np:hasProvenance
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_provenance
;
np:hasPublicationInfo
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_assertion
a
np:Assertion
.
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_provenance
a
np:Provenance
.
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_assertion
{
miriam-gene:1031
a
ncit:C16612
.
lld:C0334590
a
ncit:C7057
.
dgn-gda:DGN8fe8bc524c257f7f1166449deed01c75
sio:SIO_000628
miriam-gene:1031
,
lld:C0334590
;
a
sio:SIO_001121
.
}
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_provenance
{
dgn-np:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_assertion
dcterms:description
"[Because the CDKN2C gene, which encodes the homologous p18INK4C cell cycle regulatory protein, maps to chromosomal band 1p32, CDKN2C is an attractive candidate for the oligodendroglioma suppressor gene on chromosome 1.]. 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:10517502
;
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:NP730016.RA-hnDt3-K8Vcn0ExiA-uAZLLTsQ3eoy0CcmnOXu-fq1U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}