@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc
> .
@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:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_head
{
this:
np:hasAssertion
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_assertion
;
np:hasProvenance
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_provenance
;
np:hasPublicationInfo
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_assertion
a
np:Assertion
.
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_provenance
a
np:Provenance
.
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_assertion
{
miriam-gene:6469
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGN7da8e16019153f151df20ec7b78ab348
sio:SIO_000628
miriam-gene:6469
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_provenance
{
dgn-np:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_assertion
dcterms:description
"[We concluded that the decreased expression of the Shh pathway in atrophic gastritis and gastric cancer might reflect altered differentiation processes within the gastric unit and contributes to the development of gastric atrophy.]. 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:14691301
;
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:NP436888.RAviJCEbUqmBPbaFzD12SU2W51eUgkWyGgzrUNDlOI0Nc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}