@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8
> .
@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:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_head
{
this:
np:hasAssertion
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_assertion
;
np:hasProvenance
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_provenance
;
np:hasPublicationInfo
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_assertion
a
np:Assertion
.
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_provenance
a
np:Provenance
.
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_assertion
{
miriam-gene:7039
a
ncit:C16612
.
lld:C0206754
a
ncit:C7057
.
dgn-gda:DGNfe5399057d6ed5684c9c64c064729e02
sio:SIO_000628
miriam-gene:7039
,
lld:C0206754
;
a
sio:SIO_001121
.
}
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_provenance
{
dgn-np:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_assertion
dcterms:description
"[For example, foregut NETs have frequent deletions and mutations of the MEN1 gene, whereas midgut NETs have losses of chromosome 18, 11q and 16q and hindgut NETs express transforming growth factor-alpha and the epidermal growth factor receptor.]. 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:14713256
;
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:NP739970.RAfInhmUVuN4B3br3X0aRBwq1QhYpvvBMW_i_cdgKEEs8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:29+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" .
}