@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8
> .
@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:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_head
{
this:
np:hasAssertion
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion
;
np:hasProvenance
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance
;
np:hasPublicationInfo
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion
a
np:Assertion
.
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance
a
np:Provenance
.
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion
{
miriam-gene:4088
a
ncit:C16612
.
lld:C0029410
a
ncit:C7057
.
dgn-gda:DGNc328435c0a838b460c09999e8739505d
sio:SIO_000628
miriam-gene:4088
,
lld:C0029410
;
a
sio:SIO_001121
.
}
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_provenance
{
dgn-np:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_assertion
dcterms:description
"[Our data indicate that genetic variation in the SMAD3 gene is involved in the risk of both hip OA and knee OA in European populations, confirming the results from animal models on the potential importance of this molecule in the pathogenesis of OA.]. 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:20506137
;
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:NP294897.RAekpP8KNOPreqwuckIkStuI8G-IehRxf6hFxrkWe-7j8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}