@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk
> .
@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:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_head
{
this:
np:hasAssertion
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion
;
np:hasProvenance
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance
;
np:hasPublicationInfo
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion
a
np:Assertion
.
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance
a
np:Provenance
.
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN0c3d08c099b2e3d8f941fea90ea08688
sio:SIO_000628
miriam-gene:3126
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_provenance
{
dgn-np:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_assertion
dcterms:description
"[Although the difference in median birth weight was only 40 g, it may be considered significant because it appeared after segregation of the infants into two groups according to the single HLA class II allele group earlier associated with protection against, for example, childhood type 1 diabetes and certain infectious diseases.]. 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:15009177
;
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:NP169876.RAOc0Pd2CvNWqd8YkspNXjlPrr0EZa74uvq_oixFDfnCk130_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" .
}