@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8
> .
@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/v4.0.0/void/
> .
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_head
{
this:
np:hasAssertion
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_assertion
;
np:hasProvenance
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_assertion
a
np:Assertion
.
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_provenance
a
np:Provenance
.
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_assertion
{
miriam-gene:3908
a
ncit:C16612
.
lld:C0699743
a
ncit:C7057
.
dgn-gda:DGN86b29d6382ba2ec2e13729d927221c79
sio:SIO_000628
miriam-gene:3908
,
lld:C0699743
;
a
sio:SIO_001121
.
}
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_provenance
{
dgn-np:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_assertion
dcterms:description
"[Because approximately half of all patients with the classical form of congenital muscular dystrophy also lack merosin, availability of this animal has revived interest in the study of the pathologic mechanism of fiber necrosis resulting from this membrane defect.]. 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:9517883
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1391544.RAww2s2O-GWnjJuEQ9KChEJXi5vMhd9l7bENQ0wCUNta8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:17+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}