@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ
> .
@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:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_head
{
this:
np:hasAssertion
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_assertion
;
np:hasProvenance
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_assertion
a
np:Assertion
.
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_provenance
a
np:Provenance
.
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_assertion
{
miriam-gene:79811
a
ncit:C16612
.
lld:C0238463
a
ncit:C7057
.
dgn-gda:DGN3f8fc98a48067c5a42f3ad0f6ea3b7e8
sio:SIO_000628
miriam-gene:79811
,
lld:C0238463
;
a
sio:SIO_001121
.
}
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_provenance
{
dgn-np:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_assertion
dcterms:description
"[Although the formation of PTC is believed to result from rearrangements of RET or TRK oncogenes or MET point mutations, these structural aberrations or point mutations do not correlate with the clinicopathological features of PTC and do not seem to be a useful prognostic marker of the disease.]. 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:17201587
;
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:NP672711.RAJcAKbH2s468nJ6pHzJFSl5jJ76bWw90ao5ZqRDFcLXQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:46+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" .
}