@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8
> .
@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:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_head
{
this:
np:hasAssertion
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_assertion
;
np:hasProvenance
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_assertion
a
np:Assertion
.
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_provenance
a
np:Provenance
.
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_assertion
{
miriam-gene:2520
a
ncit:C16612
.
lld:C2939419
a
ncit:C7057
.
dgn-gda:DGNfedd4d2046aaea562704d1c41fe2bb18
sio:SIO_000628
miriam-gene:2520
,
lld:C2939419
;
a
sio:SIO_001121
.
}
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_provenance
{
dgn-np:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_assertion
dcterms:description
"[Poor prognostic factors included higher fasting gastrin levels, presence of other functional hormonal syndromes, need for >3 parathyroidectomies, presence of liver metastases or distant metastases, aggressive PET growth, large PETs, or the development of new lesions.The results of this study have helped define the causes of death of MEN1 patients at present, and have enabled us to identify a number of prognostic factors that should be helpful in tailoring treatment for these patients for both short- and long-term management, as well as in directing research efforts to better define the natural history of the disease and the most important factors determining long-term survival at present.]. 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:23645327
;
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:NP892061.RAR4n34PgcUL7Urc9OpWbk2mLeXe-E6lyUE0j49h0-G-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}