@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA
> .
@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:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_head
{
this:
np:hasAssertion
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_assertion
;
np:hasProvenance
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_assertion
a
np:Assertion
.
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_provenance
a
np:Provenance
.
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN3de72b9dd16aca8215c711adda052355
sio:SIO_000628
miriam-gene:4709
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_provenance
{
dgn-np:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_assertion
dcterms:description
"[In this study, the risk of being a DS case or having a DS child (case mother) was studied by multiple logistic regression analysis of the independent and combined genotypes and of plasma homocysteine, folates, and vitamin B12 in 92 DS cases and 140 control subjects as well as in 63 case mothers and 72 age-matched control mothers from Sicily.]. 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:12923861
;
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:NP926197.RAaWg9448YET-rHxyqbAEp3Oe9anLoXMXxwYOM7ZE1sAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}