@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g
> .
@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:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_head
{
this:
np:hasAssertion
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_assertion
;
np:hasProvenance
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_assertion
a
np:Assertion
.
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_provenance
a
np:Provenance
.
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN238d4aa2f2c290bc77f595fa10b69128
sio:SIO_000628
miriam-gene:4524
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_provenance
{
dgn-np:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_assertion
dcterms:description
"[(1) When men and women were assessed together, the frequencies of the MTHFR C677T and A1298 genotypes or their alleles were not significantly different between controls and colon cancer or rectal cancer cases.]. 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:18712959
;
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:NP320607.RA1y-Q8bfS0J4YFf6VZn1t465ozqiKjsqzdcBdJKGxf_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}