@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4
> .
@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:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_head
{
this:
np:hasAssertion
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion
;
np:hasProvenance
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion
a
np:Assertion
.
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance
a
np:Provenance
.
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion
{
miriam-gene:4650
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN24bb5d3f8ab652a0ded6b671b1fce822
sio:SIO_000628
miriam-gene:4650
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_provenance
{
dgn-np:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_assertion
dcterms:description
"[To date, seven studies have provided evidence for an association between the gene encoding for myosin IXB (MYO9B) and celiac disease (CD), and inflammatory bowel diseases, including single nucleotide polymorphisms (SNPs) rs2305767, rs1457092, and rs2305764.]. 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:20303373
;
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:NP573849.RA8aTMpPnChh9q7vso13LxYUzP_ufY-k_SOeW_b6ZeHI4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}