@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw
> .
@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:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_head
{
this:
np:hasAssertion
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_assertion
;
np:hasProvenance
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_assertion
a
np:Assertion
.
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_provenance
a
np:Provenance
.
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0410174
a
ncit:C7057
.
dgn-gda:DGN66cb55d1faaeb756d3acf79ade1376f5
sio:SIO_000628
miriam-gene:1756
,
lld:C0410174
;
a
sio:SIO_001121
.
}
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_provenance
{
dgn-np:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_assertion
dcterms:description
"[Duchenne muscular dystrophy (DMD) is caused by the defect of dystrophin, and Fukuyama congenital muscular dystrophy (FCMD) is caused by an abnormal fukutin gene leading to the glycosylation defect of alpha-dystroglycan.]. 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:20199207
;
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:NP797489.RA-E0ajlsDbYyFLOJhthTjv8A5QEfG3HvI6HjZBDhNDVw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:46+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" .
}