@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I
> .
@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:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_head
{
this:
np:hasAssertion
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_assertion
;
np:hasProvenance
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_provenance
;
np:hasPublicationInfo
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_assertion
a
np:Assertion
.
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_provenance
a
np:Provenance
.
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0262587
a
ncit:C7057
.
dgn-gda:DGNad3b4cd46adc69541f82c392f1ee2248
sio:SIO_000628
miriam-gene:4221
,
lld:C0262587
;
a
sio:SIO_001121
.
}
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_provenance
{
dgn-np:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_assertion
dcterms:description
"[Thus, we conclude that an alteration of the MEN1 gene and/or another tumor suppressor gene located at the MEN1 locus on chromosome 11q13 may be responsible for the development of parathyroid adenoma and breast cancer in our patient suggesting that the clinical spectrum of MEN1 might include breast cancer.]. 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:15168774
;
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:NP443826.RAQssWS5HfbblgO2Mn44Z84mQpWtMwCaMMcrvcUBO0X5I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}