@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw
> .
@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:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_head
{
this:
np:hasAssertion
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion
;
np:hasProvenance
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance
;
np:hasPublicationInfo
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion
a
np:Assertion
.
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance
a
np:Provenance
.
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0206754
a
ncit:C7057
.
dgn-gda:DGN262050fd773f065433e2d1aea7778fa5
sio:SIO_000628
miriam-gene:673
,
lld:C0206754
;
a
sio:SIO_001121
.
}
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_provenance
{
dgn-np:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_assertion
dcterms:description
"[We compared clinicopathological features and loss of heterozygosity of chromosomes 11q, 16q and 18, and BRAF gene mutations in 47 patients with neuroendocrine tumors including 16 with pancreatic endocrine tumors, 15 with nonileal carcinoid tumors and 16 with ileal carcinoid tumors.]. 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:15920555
;
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:NP296917.RAd0NcaWtsjIxbChjrBwyr44zQl0uvXoS6bMkLJAPnzuw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:48+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" .
}