@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs
> .
@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:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_head
{
this:
np:hasAssertion
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion
;
np:hasProvenance
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance
;
np:hasPublicationInfo
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion
a
np:Assertion
.
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance
a
np:Provenance
.
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion
{
miriam-gene:4163
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN761619ea8daaaf5daaf96f3d8348e90f
sio:SIO_000628
miriam-gene:4163
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_provenance
{
dgn-np:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_assertion
dcterms:description
"[In the present study we analyzed the association of genotype and haplotype status of two single nucleotide polymorphisms (SNPs), rs2229992 and rs11283943, in the APC and MCC genes, respectively, with an increased risk of breast carcinogenesis in a breast cancer and control population from eastern India.]. 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:21279955
;
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:NP701749.RAiMqv9lOwbfDXUGgLhr22aJZynaKktRRSgbsyhNx8Whs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}