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http://rdf.disgenet.org/nanopublications.trig#NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_assertion
;
np:hasProvenance
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_provenance
a
np:Provenance
.
dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_publicationInfo
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dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0206695
a
ncit:C7057
.
dgn-gda:DGN22d98fbd64aec0c0e014b44653b1a918
sio:SIO_000628
miriam-gene:64127
,
lld:C0206695
;
a
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.
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dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_provenance
{
dgn-np:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_assertion
dcterms:description
"[We determined the CD14 C-260T, TLR4 A +896G, C +1196T, and CARD15 G +2722C, C +2104T, 3020insC functional SNPs in dried blood samples from 118 VLBW infants (of those, 41 developed NEC) and from 146 healthy term newborns using polymerase chain reaction and restriction fragment length polymorphism methods.]. 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:16385250
;
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:NP687827.RAjXVlRejIaFqwGGdqL-RckzOs429R9o-qekMJML3F9wk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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}