@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_head
{
this:
np:hasAssertion
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_assertion
;
np:hasProvenance
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_assertion
a
np:Assertion
.
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_provenance
a
np:Provenance
.
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_assertion
{
miriam-gene:799
a
ncit:C16612
.
lld:C0029453
a
ncit:C7057
.
dgn-gda:DGNde12d264d11945e141e2649f0372099f
sio:SIO_000628
miriam-gene:799
,
lld:C0029453
;
a
sio:SIO_001122
.
}
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_provenance
{
dgn-np:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_assertion
dcterms:description
"[ Our results suggest possible connection of the AluI polymorphism of the CTR gene with osteopenia and osteoporosis development. To confirm this tendency further investigations in the large number population are necessary.]. 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:16363366
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP57844.RA8wqh84siRbjILdicdf8z2aie7dnhE5TV2-09_MV2wF4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:11+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}