@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo
> .
@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:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_head
{
this:
np:hasAssertion
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_assertion
;
np:hasProvenance
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_provenance
;
np:hasPublicationInfo
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_assertion
a
np:Assertion
.
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_provenance
a
np:Provenance
.
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_assertion
{
miriam-gene:632
a
ncit:C16612
.
lld:C0020630
a
ncit:C7057
.
dgn-gda:DGN82753b2756f5ca183a8f38f4cdb94d75
sio:SIO_000628
miriam-gene:632
,
lld:C0020630
;
a
sio:SIO_001121
.
}
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_provenance
{
dgn-np:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_assertion
dcterms:description
"[Because defective bone mineralization occurs in hypophosphatasia (HP) and the source of bone alkaline phosphatase is the osteoblast, we investigated another marker of osteoblast activity, namely the production of osteocalcin in an HP family and controls.]. 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:1793676
;
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:NP439726.RA80TrEm6mGJZBnG3bHIiBwSNSix9VYsi7eUM39TafCXo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}