@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s
> .
@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/v4.0.0/void/
> .
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_head
{
this:
np:hasAssertion
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_assertion
;
np:hasProvenance
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_provenance
;
np:hasPublicationInfo
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_assertion
a
np:Assertion
.
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_provenance
a
np:Provenance
.
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN7df11095c6931f01198517e60c863f7a
sio:SIO_000628
miriam-gene:64127
,
lld:C0021390
;
a
sio:SIO_001122
.
}
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_provenance
{
dgn-np:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_assertion
dcterms:description
"[Unfortunately, even if the association between the three main CARD15 mutations (R702W, G908R and 1007fs) and CD is clearly established, it is not useful today to genotype asymptomatic at risk people or inflammatory bowel disease patients as a routine.]. 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:12840668
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP400402.RAlNA-ehKX_tWr94NKGUmC6O-7a7bCWWiClBOvJLI6m9s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:46+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: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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}