@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI
> .
@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/v3.0.0/void/
> .
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_head
{
this:
np:hasAssertion
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_assertion
;
np:hasProvenance
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_provenance
;
np:hasPublicationInfo
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_assertion
a
np:Assertion
.
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_provenance
a
np:Provenance
.
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN9de5fdd39078bb9a6a3b3cf5ec154cf4
sio:SIO_000628
miriam-gene:4548
,
lld:C0010054
;
a
sio:SIO_001122
.
}
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_provenance
{
dgn-np:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP577235.RAeda0iHYukPXbVEps4dpwKdznzGHKQeZGiiZl_aJ6XZI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:24+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}