@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE
> .
@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:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_head
{
this:
np:hasAssertion
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_assertion
;
np:hasProvenance
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_assertion
a
np:Assertion
.
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_provenance
a
np:Provenance
.
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGNe11d3931a04e96ff22ecb9d90264e74c
sio:SIO_000628
miriam-gene:4524
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_provenance
{
dgn-np:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_assertion
dcterms:description
"[Previous studies have shown that homocysteine level and the C677T polymorphism in the gene encoding methylenetetrahydrofolate reductase (MTHFR) may be involved in the development of osteoporosis and its related fracture in European populations.]. 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:17174622
;
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:NP885633.RAZrf6Ajy52Gxey3UZHE6oZ-4wYSkdKyRS2gnMiKKDBFE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:01+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" .
}