@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig
> .
@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:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_head
{
this:
np:hasAssertion
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_assertion
;
np:hasProvenance
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_provenance
;
np:hasPublicationInfo
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_assertion
a
np:Assertion
.
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_provenance
a
np:Provenance
.
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN96e0e1476c3186f2591a35d333a81790
sio:SIO_000628
miriam-gene:189
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_provenance
{
dgn-np:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_assertion
dcterms:description
"[The M235T polymorphism, which influences AGT gene expression, was evaluated by restriction fragment length polymorphism analysis in the DNA samples of 163 German and Greek patients with oral squamous cell carcinoma (OSCC) and 124 healthy controls of equivalent gender, ethnicity and age.]. 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:18630525
;
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:NP550262.RAI0IYVR1Zqv31FGwlO1avLy_LBxg7WwEtGIJc_lWLJig130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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: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" .
}