@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU
> .
@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:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_head
{
this:
np:hasAssertion
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_assertion
;
np:hasProvenance
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_provenance
;
np:hasPublicationInfo
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_assertion
a
np:Assertion
.
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_provenance
a
np:Provenance
.
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0005940
a
ncit:C7057
.
dgn-gda:DGNe9479271de12f7e35dac47cf51c11f6e
sio:SIO_000628
miriam-gene:1756
,
lld:C0005940
;
a
sio:SIO_001121
.
}
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_provenance
{
dgn-np:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_assertion
dcterms:description
"[In contrast, significant advances have been made in identifying the genes that cause monogenic bone diseases, and polymorphic variation is some of these genes has been found to contribute to the genetic regulation of BMD in the normal 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:17288970
;
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:NP899672.RACGSjwPB2O0GzNBswp5wAVmZ_AXQBY5InfWvzdD_JcLU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}