@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU
> .
@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:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_head
{
this:
np:hasAssertion
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_assertion
;
np:hasProvenance
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_assertion
a
np:Assertion
.
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_provenance
a
np:Provenance
.
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_assertion
{
miriam-gene:3998
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN1524a55520c766ca32eddcb13324d211
sio:SIO_000628
miriam-gene:3998
,
lld:C0021390
;
a
sio:SIO_001122
.
}
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_provenance
{
dgn-np:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_assertion
dcterms:description
"[These results suggest that MBL mutations which decrease the formation of functional MBL could protect against the clinical development of sporadic UC, but not of CD. This could be explained by the differential T-helper response in both diseases.]. 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:11607788
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP71703.RAUCCdQhGzQERx_eUHA4OEFlGGvZqJB5u67hXgQHcCwUU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:20+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}