@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po
> .
@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:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_head
{
this:
np:hasAssertion
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_assertion
;
np:hasProvenance
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_provenance
;
np:hasPublicationInfo
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_assertion
a
np:Assertion
.
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_provenance
a
np:Provenance
.
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0005940
a
ncit:C7057
.
dgn-gda:DGN8a5d7e82f4870a49c0f53ba388e289b7
sio:SIO_000628
miriam-gene:2778
,
lld:C0005940
;
a
sio:SIO_001121
.
}
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_provenance
{
dgn-np:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_assertion
dcterms:description
"[The apparently contradictory results in women and men and the finding that the GNAS1 T393C genotype is an independent factor for time to aseptic loosening in male patients assigned this polymorphism as an interesting target for further investigations in bone diseases.]. 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:18634020
;
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:NP683639.RAruXg5EnzTt1m9EHiETnrS4zxMVS-MKNCrXElAdZk3Po130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}