@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ
> .
@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:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_head
{
this:
np:hasAssertion
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_assertion
;
np:hasProvenance
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_assertion
a
np:Assertion
.
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_provenance
a
np:Provenance
.
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN9650fa70e21a49ed6d2eba2236d082d3
sio:SIO_000628
miriam-gene:4524
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_provenance
{
dgn-np:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_assertion
dcterms:description
"[The MTHFR C677T polymorphism shows no consistent correlation with cardiovascular risk and longevity but, in combination with positive folate balance, the TT genotype is associated with decreased risk of colorectal neoplasias.]. 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:11282420
;
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:NP435946.RAc9A3LkVcdQQXxIw6PyQ3Mb1-L_0_XyXx9VJBSWlW6hQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}