@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg
> .
@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:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_head
{
this:
np:hasAssertion
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_assertion
;
np:hasProvenance
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_provenance
;
np:hasPublicationInfo
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_assertion
a
np:Assertion
.
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_provenance
a
np:Provenance
.
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNb12fe4fcc19f7fa2f90086055ffa83cc
sio:SIO_000628
miriam-gene:4709
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_provenance
{
dgn-np:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_assertion
dcterms:description
"[Individuals with a family history of diabetes or with risk factors such as obesity, hypertension, and impaired glucose tolerance should be screened for MTHFR C677T mutation and may be prescribed folic acid, vitamin B6, and vitamin B12 to assess if this helps in delaying the onset of diabetes.]. 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:21186995
;
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:NP791530.RArrtkalRR8swySfhpMBhkw2YUlolMTTXBR9S0CXJUnvg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}