@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_head
{
this:
np:hasAssertion
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_assertion
;
np:hasProvenance
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_provenance
;
np:hasPublicationInfo
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_assertion
a
np:Assertion
.
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_provenance
a
np:Provenance
.
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0270984
a
ncit:C7057
.
dgn-gda:DGN12f3ed3a4d85ca3bdca639489a967cdf
sio:SIO_000628
miriam-gene:270
,
lld:C0270984
;
a
sio:SIO_001121
.
}
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_provenance
{
dgn-np:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_assertion
dcterms:description
"[Consequently, genetic tests for abnormal AMPD1 expression designed to diagnose patients with metabolic myopathy, and to evaluate genetic markers for clinical outcome in heart disease should not be based solely on the detection of a single mutant allele.]. 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:12117480
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP237670.RALx7vrTUYeBMHv2UjV8kN8CwxiotyfbKFHK2i42FUtyc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:55+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}