@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc
> .
@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:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_head
{
this:
np:hasAssertion
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_assertion
;
np:hasProvenance
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_provenance
;
np:hasPublicationInfo
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_assertion
a
np:Assertion
.
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_provenance
a
np:Provenance
.
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007113
a
ncit:C7057
.
dgn-gda:DGNc67003125bfd0c51d2fd6a298925e1d3
sio:SIO_000628
miriam-gene:4524
,
lld:C0007113
;
a
sio:SIO_001121
.
}
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_provenance
{
dgn-np:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_assertion
dcterms:description
"[The present study did not find a reduced risk of colorectal or rectal cancer among those with a variant genotype of the MTHFR polymorphism, but observed rather an increased risk of colon cancer, suggesting that the effects of the MTHFR genotype may differ in populations with different levels of folate intake.]. 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:15533596
;
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:NP404749.RAXn3vZFWYtSwxZFhWnA1xy1YpP-KE4tvtjN1caBFFewc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}