@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw
> .
@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:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_head
{
this:
np:hasAssertion
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_assertion
;
np:hasProvenance
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_assertion
a
np:Assertion
.
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_provenance
a
np:Provenance
.
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_assertion
{
miriam-gene:5726
a
ncit:C16612
.
lld:C0342208
a
ncit:C7057
.
dgn-gda:DGNbd74cba1ba4ba3ff8b3e312ecb500a7d
sio:SIO_000628
miriam-gene:5726
,
lld:C0342208
;
a
sio:SIO_001121
.
}
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_provenance
{
dgn-np:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_assertion
dcterms:description
"[The second group includes familial syndromes characterized by predominance of papillary thyroid carcinoma (PTC), such as pure familial PTC (fPTC), fPTC associated with papillary renal cell carcinoma, and fPTC with multinodular goiter.]. 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:21455198
;
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:NP636242.RA0AMIV53eP7tTzaIR7vsmVPkCkl3O3I8nBWfIESN0aBw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}