@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8
> .
@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:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_head
{
this:
np:hasAssertion
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion
;
np:hasProvenance
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance
;
np:hasPublicationInfo
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion
a
np:Assertion
.
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance
a
np:Provenance
.
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion
{
miriam-gene:4502
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN3dd3ba17af2cafaff4fcee8027a0dccf
sio:SIO_000628
miriam-gene:4502
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_provenance
{
dgn-np:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_assertion
dcterms:description
"[Using the PCR-based restriction fragment length polymorphism method, seven single nucleotide polymorphisms (SNPs) in MT genes (rs8052394 and rs11076161 in MT1A gene, rs8052334, rs964372, and rs7191779 in MT1B gene, rs708274 in MT1E gene, and rs10636 in MT2A gene) were detected in 851 Chinese people of Han descent (397 diabetes and 454 controls).]. 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:18349110
;
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:NP572151.RASuxw0GBHqlVr9XbVkgZlThXMXjjeYX-2d79QJqiF6r8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}