@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI
> .
@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:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_head
{
this:
np:hasAssertion
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_assertion
;
np:hasProvenance
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_provenance
;
np:hasPublicationInfo
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_assertion
a
np:Assertion
.
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_provenance
a
np:Provenance
.
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN078d1e4e85a162bf6e03fd8af0dcf52a
sio:SIO_000628
miriam-gene:7421
,
lld:C0024117
;
a
sio:SIO_001122
.
}
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_provenance
{
dgn-np:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_assertion
dcterms:description
"[The FokI common variants in the VDR gene are associated with skeletal muscle strength in both patients and control subjects, whereas the BsmI polymorphism is associated with strength only in patients.]. 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:18258629
;
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:NP79943.RANpyFc6EzCNgIndyIXLjARnvmBeD-a-Sf_Yc3-uMxdiI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:39+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" .
}