@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A
> .
@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:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_head
{
this:
np:hasAssertion
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_assertion
;
np:hasProvenance
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_provenance
;
np:hasPublicationInfo
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_assertion
a
np:Assertion
.
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_provenance
a
np:Provenance
.
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0271623
a
ncit:C7057
.
dgn-gda:DGN430c0aa30f1e6007ccc23a36f2a3aa82
sio:SIO_000628
miriam-gene:1756
,
lld:C0271623
;
a
sio:SIO_001121
.
}
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_provenance
{
dgn-np:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_assertion
dcterms:description
"[No differences in BMD were seen between control subgroups, but total femur and femoral neck BMD were significantly lower in patients bearing heterozygous Ff genotype with IHH than homozygous FF ones (p=0.017 and p=0.009, respectively).]. 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:16370560
;
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:NP403498.RAdXNzo_s48H10q8H7DaneTf93E4wsoyh2vaULEH1yn7A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}