@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE
> .
@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:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_head
{
this:
np:hasAssertion
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_assertion
;
np:hasProvenance
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_assertion
a
np:Assertion
.
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_provenance
a
np:Provenance
.
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNdd56f41a7d10aa4864023a4ab7cb5bb1
sio:SIO_000628
miriam-gene:875
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_provenance
{
dgn-np:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_assertion
dcterms:description
"[Our results suggest that neither single mutation nor combined mutations in MTHFR C677T, CBS 844ins68 and MS A2756G represent an independent risk factor for increasing IS and coronary artery disease risks in Chinese population.]. 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:11672761
;
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:NP371517.RAb9c12gYzxnx8a7IFef2W7wS9x8e8PDphehyOzBq6qhE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}