@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM
> .
@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:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_head
{
this:
np:hasAssertion
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_assertion
;
np:hasProvenance
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_assertion
a
np:Assertion
.
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_provenance
a
np:Provenance
.
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGNb850bbad7cc7bdfe8793b61d017f2567
sio:SIO_000628
miriam-gene:7015
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_provenance
{
dgn-np:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_assertion
dcterms:description
"[Our group has recently demonstrated that patients with FPTC have shorter telomeres, not associated with mutations in telomerase reverse transcriptase, gene than patients with sporadic papillary thyroid cancer (SPTC), healthy subjects (HS), and unaffected family members (UFMs).]. 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:22304389
;
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:NP572466.RAVk7u2ohESNR_4UznIOVJe9sXWxQcLEEykOj2Xd_uTmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}