@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE
> .
@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:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_head
{
this:
np:hasAssertion
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion
;
np:hasProvenance
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion
a
np:Assertion
.
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance
a
np:Provenance
.
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion
{
miriam-gene:3578
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGN50a66ba80864b3fddd0004b6a68af4c9
sio:SIO_000628
miriam-gene:3578
,
lld:C0007570
;
a
sio:SIO_001122
.
}
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_provenance
{
dgn-np:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_assertion
dcterms:description
"[There were no statistically significant allele or haplotype frequency differences between cases and controls. Therefore, these results provide no evidence that these loci are associated with CD in this sample population.]. 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:15713213
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55944.RAb0UL0hOnMyLjyYDkJRKEs1Zh0mCryHEtEaqlThKZvZE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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" .
}