@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs
> .
@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:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_head
{
this:
np:hasAssertion
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion
;
np:hasProvenance
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance
;
np:hasPublicationInfo
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion
a
np:Assertion
.
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance
a
np:Provenance
.
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion
{
miriam-gene:353322
a
ncit:C16612
.
lld:C0238288
a
ncit:C7057
.
dgn-gda:DGNc200cb7b7c37dfc10b311f535ae2a22d
sio:SIO_000628
miriam-gene:353322
,
lld:C0238288
;
a
sio:SIO_001121
.
}
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_provenance
{
dgn-np:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_assertion
dcterms:description
"[The aim of this study is to comprehensively and uniformly study the expression of the FSHD candidate genes FRG1, FRG2, CRYM, ANT1, ALP, PITX1 and LRP2BP at the RNA and protein level in identically processed primary myoblasts, myotubes and quadriceps muscle.]. 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:19809486
;
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:NP815109.RAMuqHgzNFEpbXkoClvQ4JfCSOK45hBRBVV7pYaHd_eHs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}