@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto
> .
@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 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:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_head
{
this:
np:hasAssertion
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_assertion
;
np:hasProvenance
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_provenance
;
np:hasPublicationInfo
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_assertion
a
np:Assertion
.
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_provenance
a
np:Provenance
.
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGN41cdde5016e69d0a77eeae13f2fd40db
sio:SIO_000628
miriam-gene:5728
,
lld:C0007115
;
a
sio:SIO_001121
.
}
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_provenance
{
dgn-np:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_assertion
dc:description
"[In this study, we confirm that PTEN mutations in sporadic thyroid cancer are infrequent as we found one point mutation and one heterozygous deletion of PTEN gene in 26 tumors and eight cell lines screened.]. 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:10918569
;
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:NP380381.RAD6CR3Uxu_hAqkI_tZOIaopdmMmAcDiuOQyLm4Wc4Rto130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:45+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}