@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_head
{
this:
np:hasAssertion
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_assertion
;
np:hasProvenance
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_provenance
;
np:hasPublicationInfo
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_assertion
a
np:Assertion
.
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_provenance
a
np:Provenance
.
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007104
a
ncit:C7057
.
dgn-gda:DGNe0ffa6ae95fc16c409bc80175acf2e4f
sio:SIO_000628
miriam-gene:4524
,
lld:C0007104
;
a
sio:SIO_001121
.
}
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_provenance
{
dgn-np:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_assertion
dcterms:description
"[In conclusion, our study provides support to account for the preferential role of cSHMT polymorphism to lower risk of female breast cancer, and such reduced risk would be more significant in carriers with the polymorphisms of MS and MTHFR genes.]. 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:17896178
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP631927.RAFQafL24gfes0WbPmoOFShrYURIOtZqD624V8mcKIUCs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:32+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}