@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs
> .
@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:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_head
{
this:
np:hasAssertion
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_assertion
;
np:hasProvenance
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_provenance
;
np:hasPublicationInfo
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_assertion
a
np:Assertion
.
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_provenance
a
np:Provenance
.
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_assertion
{
miriam-gene:201163
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGNbfdcdbf15c4205fdce4578edc775df78
sio:SIO_000628
miriam-gene:201163
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_provenance
{
dgn-np:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_assertion
dcterms:description
"[To test the hypothesis that the BHD gene is also a mutational target in sporadic endometrial carcinoma with microsatellite instability, 139 cases of sporadic endometrial carcinoma were screened for MSI status, and mutations of the poly(C)8 tract in exon 11 as well as other coding exons of the BHD gene.]. 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:16691634
;
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:NP554514.RAxjTKe3mfDUER19naWuw8Z6CVfqs-4PuHwtDtCn9pyvs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}