@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c
> .
@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:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_head
{
this:
np:hasAssertion
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_assertion
;
np:hasProvenance
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_provenance
;
np:hasPublicationInfo
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_assertion
a
np:Assertion
.
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_provenance
a
np:Provenance
.
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_assertion
{
miriam-gene:3560
a
ncit:C16612
.
lld:C0038013
a
ncit:C7057
.
dgn-gda:DGNc124ebfb6b6851652d01f3b545868335
sio:SIO_000628
miriam-gene:3560
,
lld:C0038013
;
a
sio:SIO_001121
.
}
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_provenance
{
dgn-np:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_assertion
dcterms:description
"[Polymorphisms associated in the allele frequencies test with severe BASFI/t in all classifications were: rs2542151 (p60 [P = .04], p65 [P = .04], p70 [P = .001] and p75 [P = .001]) and rs2254441 (p60 [P = .004], p65 [P = .02], p70 [P = .01] and p75 [P<.001]).. Genotype association, after adjustment for covariates, found an association in three of the four patients' classifications for rs2542151 and in two of the classifications for rs2254441.Forward logistic regression did not identify any model with a good predictive power for severe functional development.In our study we identified clinical factors and 24 polymorphisms associated with development of severe functional status in AS patients.]. 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:22984424
;
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:NP170195.RAVKpMnv4PCUbUNBijPFXu7Q6CWRY_kL0iVcazUIrX43c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}