@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo
> .
@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:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_head
{
this:
np:hasAssertion
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_assertion
;
np:hasProvenance
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_assertion
a
np:Assertion
.
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_provenance
a
np:Provenance
.
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_assertion
{
miriam-gene:2212
a
ncit:C16612
.
lld:C0031099
a
ncit:C7057
.
dgn-gda:DGNecdca7f24ccad0ebd962a1cd0090181c
sio:SIO_000628
miriam-gene:2212
,
lld:C0031099
;
a
sio:SIO_001122
.
}
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_provenance
{
dgn-np:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_assertion
dcterms:description
"[The results are evidence that the FcgammaRIIIa genotype coding for the high affinity receptor imposes an additional risk of bone loss as does the FcgammaRIIIb genotype coding for the low affinity receptor.]. 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:11528518
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44121.RANhLKxN-3U0agpmnczxRJYhudG-e-su-XCyfv_reyPLo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}