@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ
> .
@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:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_head
{
this:
np:hasAssertion
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion
;
np:hasProvenance
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion
a
np:Assertion
.
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance
a
np:Provenance
.
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0745106
a
ncit:C7057
.
dgn-gda:DGN633b62e20c07fd7da56613c43e4c23bf
sio:SIO_000628
miriam-gene:2778
,
lld:C0745106
;
a
sio:SIO_001121
.
}
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_provenance
{
dgn-np:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_assertion
dcterms:description
"[Osteomalacic and hyperparathyroid changes, which emanate from distinct metabolic derangements (which superimpose on the local effects of GNAS1 mutations in bone), influence, in turn, the severity and type of skeletal morbidity in FD.]. 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:12854833
;
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:NP832539.RAHRd0TVvT8GREgXjGeM7Li4KiHS_hs2GZNrvmc8u9XIQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}