@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE
> .
@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:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_head
{
this:
np:hasAssertion
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_assertion
;
np:hasProvenance
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_provenance
;
np:hasPublicationInfo
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_assertion
a
np:Assertion
.
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_provenance
a
np:Provenance
.
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_assertion
{
miriam-gene:4650
a
ncit:C16612
.
lld:C0009324
a
ncit:C7057
.
dgn-gda:DGN3acbadadd9184e5731bba8ca86664a09
sio:SIO_000628
miriam-gene:4650
,
lld:C0009324
;
a
sio:SIO_001121
.
}
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_provenance
{
dgn-np:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_assertion
dcterms:description
"[Unlike previous variants (in other genes) reported to predispose to inflammatory bowel disease, the association at MYO9B was considerably stronger with ulcerative colitis, although weaker association with Crohn's disease also was observed.]. 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:17087940
;
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:NP697398.RARUqe7UZ-6WiyUmXhcfVIPmWX8cJ3AylbqsCUImE7GbE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}