@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_head
{
this:
np:hasAssertion
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_assertion
;
np:hasProvenance
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_provenance
;
np:hasPublicationInfo
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_assertion
a
np:Assertion
.
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_provenance
a
np:Provenance
.
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_assertion
{
miriam-gene:4485
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN76a9548289aa365c8656966d764d3277
sio:SIO_000628
miriam-gene:4485
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_provenance
{
dgn-np:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_assertion
dcterms:description
"[A non-synonymous coding variant in MSP (689C) has been associated with genetic susceptibility to both Crohn's disease and ulcerative colitis, two major types of inflammatory bowel disease (IBD) characterized by chronic inflammation of the digestive tract.]. 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:24409221
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP571322.RAHKABwik4aie4dOKBAtJwZ-fSYh-roTBCDJqhU-T77Ag130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:20+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}