@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc
> .
@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:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_head
{
this:
np:hasAssertion
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_assertion
;
np:hasProvenance
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_provenance
;
np:hasPublicationInfo
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_assertion
a
np:Assertion
.
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_provenance
a
np:Provenance
.
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0013274
a
ncit:C7057
.
dgn-gda:DGNdac359e369d9e1267fefc7f76d8ec4c0
sio:SIO_000628
miriam-gene:4153
,
lld:C0013274
;
a
sio:SIO_001121
.
}
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_provenance
{
dgn-np:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_assertion
dcterms:description
"[MBL gene polymorphism was associated with increased frequency of clinical sepsis particularly with early neonatal sepsis and also with higher Tollner sepsis scores and increased frequency of patent ductus arteriosus in infants.]. 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:20453525
;
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:NP720018.RA8F2hyOUT_Uw24MqsX1aIUDs0LztUk2o38yVO49qoQmc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}