@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8
> .
@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:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_head
{
this:
np:hasAssertion
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_assertion
;
np:hasProvenance
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_provenance
;
np:hasPublicationInfo
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_assertion
a
np:Assertion
.
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_provenance
a
np:Provenance
.
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C1263858
a
ncit:C7057
.
dgn-gda:DGN778e65214a760252b083fb054d11113d
sio:SIO_000628
miriam-gene:596
,
lld:C1263858
;
a
sio:SIO_001121
.
}
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_provenance
{
dgn-np:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_assertion
dcterms:description
"[Thus, BCL2-mediated apoptosis appears to play a significant role in pathogenesis of laminin alpha2 deficiency, but not of dystrophin deficiency, suggesting that therapies designed to ameliorate disease by inhibition of apoptosis are more likely to succeed in MDC1A than in DMD.]. 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:15757977
;
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:NP765805.RAtxwnbT8cIUAkKr9u6PjUp_etFiu8rE2dtvJ_Als59B8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}