@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E
> .
@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:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_head
{
this:
np:hasAssertion
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion
;
np:hasProvenance
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion
a
np:Assertion
.
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance
a
np:Provenance
.
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0747079
a
ncit:C7057
.
dgn-gda:DGN5755a41bc8f68f69b5c62d13f1a04c09
sio:SIO_000628
miriam-gene:1756
,
lld:C0747079
;
a
sio:SIO_001121
.
}
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_provenance
{
dgn-np:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_assertion
dcterms:description
"[As several non-synonymous single nucleotide polymorphisms (SNPs) have been identified within the P2Y(2) receptor gene in humans, we examined associations between genetic variations in the P2Y(2) receptor gene and bone mineral density (BMD) (i.e., osteoporosis risk), in a cohort of fracture patients.]. 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:22773251
;
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:NP658452.RAMbVoFvN5cUOFsVh5U_XIgFuZIKph44KhzdH3YP6hl0E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:36+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" .
}