@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_assertion
;
np:hasProvenance
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_provenance
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np:hasPublicationInfo
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_assertion
a
np:Assertion
.
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_provenance
a
np:Provenance
.
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3929
a
ncit:C16612
.
lld:C0036690
a
ncit:C7057
.
dgn-gda:DGNe28ac09423b90e54afe01443e87a4406
sio:SIO_000628
miriam-gene:3929
,
lld:C0036690
;
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.
}
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_provenance
{
dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_assertion
dcterms:description
"[Our findings suggest that common polymorphisms in the gene for LBP in combination with male gender are associated with an increased risk for the development of sepsis and, furthermore, may be linked to an unfavorable outcome.]. 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:11373419
;
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 .
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dgn-np:NP491613.RA-TkrqPhw4oHONpg_IwevTmDqFtoSlK9j9qM4QuKAwzU130_publicationInfo
{
this:
dcterms:created
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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
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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