@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU
> .
@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:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_head
{
this:
np:hasAssertion
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_assertion
;
np:hasProvenance
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_provenance
;
np:hasPublicationInfo
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_assertion
a
np:Assertion
.
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_provenance
a
np:Provenance
.
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGN513bf9c1904e98b5b62c07017d230131
sio:SIO_000628
miriam-gene:673
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_provenance
{
dgn-np:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_assertion
dcterms:description
"[Papillary microcarcinoma had acquired similar genomic mutations as conventional PTC, but higher frequencies of mutations of BRAF, 1p36, 18q, and 22q13 were found in the larger PTC, suggesting that they might play a role in the aggressiveness of PTC.]. 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:18628356
;
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:NP170689.RAdPSl0fFyGFLpKlZD0HVzDZkcZtkb_LfQcsa-oSyAneU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}