@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE
> .
@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:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_head
{
this:
np:hasAssertion
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_assertion
;
np:hasProvenance
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_provenance
;
np:hasPublicationInfo
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_assertion
a
np:Assertion
.
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_provenance
a
np:Provenance
.
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_assertion
{
miriam-gene:9967
a
ncit:C16612
.
lld:C0153653
a
ncit:C7057
.
dgn-gda:DGN8c01f5d6d95699882036bd8e3992e919
sio:SIO_000628
miriam-gene:9967
,
lld:C0153653
;
a
sio:SIO_001121
.
}
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_provenance
{
dgn-np:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_assertion
dcterms:description
"[Loss of the short arm of chromosome 1, along with somatic missense and truncating mutations in CDKN2C and THRAP3, respectively, provides new evidence for the potential role of these genes as tumour suppressors in parathyroid 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:23616356
;
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:NP778338.RA4TxNqWSVs9390uE4jaZAJUUHpZa8EHcumG9-FJZR8cE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}