@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y
> .
@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:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_head
{
this:
np:hasAssertion
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_assertion
;
np:hasProvenance
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_assertion
a
np:Assertion
.
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_provenance
a
np:Provenance
.
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_assertion
{
miriam-gene:4914
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN927c0914af622cdeefac6f674eb9e131
sio:SIO_000628
miriam-gene:4914
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_provenance
{
dgn-np:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_assertion
dcterms:description
"[In addition to these putative genes, a number of loci represent candidate familial nonmedullary thyroid cancer predisposition genes by virtue of their involvement in sporadic disease (TRKA), their role in benign disease (TSHR), and because they underlie syndromes with a risk of nonmedullary thyroid cancer (PTEN).]. 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:11502798
;
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:NP208779.RApj9w3g_kXHHO_WCI_1x7FaTAKo2hHRUFINKlbWmcf7Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}