@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o
> .
@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:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_head
{
this:
np:hasAssertion
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_assertion
;
np:hasProvenance
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_assertion
a
np:Assertion
.
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_provenance
a
np:Provenance
.
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNa6ab64d3add126a95be1fcc25d1b6746
sio:SIO_000628
miriam-gene:6648
,
lld:C1458155
;
a
sio:SIO_001122
.
}
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_provenance
{
dgn-np:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_assertion
dcterms:description
"[The MnSOD Ala-9Val polymorphism may contribute to an increase in breast cancer risk in the context of high alcohol consumption, however the polymorphism is not an overall risk factor for breast cancer in this primarily premenopausal 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:16933053
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP108878.RAoy8_YmufeyDhgJGKHjsGHZmCzDruW6LTPKKs-LriN8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:55+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" .
}