@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c
> .
@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:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_head
{
this:
np:hasAssertion
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion
;
np:hasProvenance
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance
;
np:hasPublicationInfo
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion
a
np:Assertion
.
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance
a
np:Provenance
.
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0021670
a
ncit:C7057
.
dgn-gda:DGNdb8b764ecc391b50bef0392b0d960846
sio:SIO_000628
miriam-gene:4221
,
lld:C0021670
;
a
sio:SIO_001121
.
}
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_provenance
{
dgn-np:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_assertion
dcterms:description
"[The lower rate of 11q13 LOH in MEN1-associated and sporadic gastrinomas and sporadic insulinomas as compared to MEN1 nongastrinomas may reflect alternative genetic pathways for the development of these tumors or mechanisms of the MEN1 gene inactivation that do not involve large deletions.]. 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:9187127
;
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:NP263334.RAdL3ACRD59nxBf_r4sofWFnfnn46KSSWlXCpBga0R99c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}