@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA
> .
@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:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_head
{
this:
np:hasAssertion
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_assertion
;
np:hasProvenance
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_provenance
;
np:hasPublicationInfo
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_assertion
a
np:Assertion
.
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_provenance
a
np:Provenance
.
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_assertion
{
miriam-gene:270
a
ncit:C16612
.
lld:C0018799
a
ncit:C7057
.
dgn-gda:DGN349fde6f4b0b0a189ec1ae34eb41df52
sio:SIO_000628
miriam-gene:270
,
lld:C0018799
;
a
sio:SIO_001121
.
}
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_provenance
{
dgn-np:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_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-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:NP487127.RAxNh7Axu8M8isRhW9rAch5Eq9ybfleSxNuZMKAOTghLA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}