@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ
> .
@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:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_head
{
this:
np:hasAssertion
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion
;
np:hasProvenance
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion
a
np:Assertion
.
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance
a
np:Provenance
.
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion
{
miriam-gene:57876
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN324d52d3a624e3b11ee95bb29b545db4
sio:SIO_000628
miriam-gene:57876
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_provenance
{
dgn-np:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_assertion
dcterms:description
"[We have also analyzed the single nucleotide polymorphisms (SNPs) in the exonic sequences of the 3' portions of these two genes to investigate whether sequence variations in these regions can cause person-to-person differences in the susceptibility to IBDs, and report here that non-synonymous SNPs of MUC3A, involving a tyrosine residue with a proposed role in cell signaling, may confer genetic predisposition to CD (P = 0.0132).]. 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:11289722
;
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:NP656488.RA3c9ZabpXhIyqB-s1saumhQrBoqrB20v1eH8St_ZyLYQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+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" .
}