@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE
> .
@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:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_head
{
this:
np:hasAssertion
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_assertion
;
np:hasProvenance
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_provenance
;
np:hasPublicationInfo
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_assertion
a
np:Assertion
.
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_provenance
a
np:Provenance
.
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGNf1b83ab14e7577ffda8c9991f50eb1c9
sio:SIO_000628
miriam-gene:64127
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_provenance
{
dgn-np:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_assertion
dcterms:description
"[These topics are (1) NOD2 variants in Crohn's disease, (2) Heliobacter pylori and CagA and VacA pathogenesis, (3) beta-catenin function in normal colonic epithelia and colon cancer, (4) DNA methylation in colonic cancer, (5) the HCV replicon, and (6) the use of small interfering RNA in somatic cell genetics.]. 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:15017626
;
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:NP361478.RAmwKle3gknSwDbdROjaSedWvyMJK3k23VoZip7ota-oE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}