@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ
> .
@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:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_head
{
this:
np:hasAssertion
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_assertion
;
np:hasProvenance
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_assertion
a
np:Assertion
.
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_provenance
a
np:Provenance
.
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0017924
a
ncit:C7057
.
dgn-gda:DGNe9ae246052d685575ad940376b359314
sio:SIO_000628
miriam-gene:270
,
lld:C0017924
;
a
sio:SIO_001121
.
}
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_provenance
{
dgn-np:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_assertion
dcterms:description
"[In summary, heterozigosity for the C34T allele of the AMPD gene is associated with reduced submaximal aerobic capacity in female patients with McArdle disease and might partly account, in this gender, for the variability that exists in the phenotypic manifestation of the disease.]. 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:17687759
;
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:NP338192.RAaq75KSK2XK54NWv-l83V7dnkHrJRagdSaw-FF6lGNmQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}