@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74
> .
@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:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_head
{
this:
np:hasAssertion
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_assertion
;
np:hasProvenance
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_provenance
;
np:hasPublicationInfo
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_assertion
a
np:Assertion
.
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_provenance
a
np:Provenance
.
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1336076
a
ncit:C7057
.
dgn-gda:DGNda323083fd44a68ae96a7b3d213e1752
sio:SIO_000628
miriam-gene:4524
,
lld:C1336076
;
a
sio:SIO_001121
.
}
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_provenance
{
dgn-np:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_assertion
dcterms:description
"[These results for MTHFR polymorphism might be population specific in sporadic breast cancer affected patients but many other factors need to be excluded before making final conclusions including folate intake, population and disease heterogeneity.]. 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:22799374
;
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:NP691883.RA9s5g5BByjD1ENpUmhl5mUtnS_QKwZBKLZV4v_2G6x74130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}