@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw
> .
@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:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_head
{
this:
np:hasAssertion
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_assertion
;
np:hasProvenance
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_provenance
;
np:hasPublicationInfo
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_assertion
a
np:Assertion
.
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_provenance
a
np:Provenance
.
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN5bfecf77638b58dc40431a0695bd58c5
sio:SIO_000628
miriam-gene:4709
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_provenance
{
dgn-np:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_assertion
dcterms:description
"[To investigate the frequencies of C677T polymorphism in MTHFR gene and G80A polymorphism in RFC gene in obese and no obese Tunisian children and to assess their relation with homocysteine (tHcy), folate and vitamin B12 levels.]. 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:21681722
;
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:NP861151.RAQpThAq9zveuE2ykaGUWpnUP8GTf8dILh5YXngNFzHzw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:46+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" .
}