@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ
> .
@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:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_head
{
this:
np:hasAssertion
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_assertion
;
np:hasProvenance
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_assertion
a
np:Assertion
.
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_provenance
a
np:Provenance
.
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN2bc688baaa5a8629a35e89a43d8a8faf
sio:SIO_000628
miriam-gene:5728
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_provenance
{
dgn-np:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_assertion
dcterms:description
"[Although somatic intragenic PTEN mutations have rarely been found in benign and malignant sporadic thyroid tumors, loss of heterozygosity (LOH) has been reported in up to one fourth of follicular thyroid adenomas (FAs) and carcinomas.]. 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:10793080
;
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:NP719246.RAXQ9Gy0nyWd0K7sjAPtW31T3jJ3lpfALeMJaXe-ilULQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}