@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME
> .
@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:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_head
{
this:
np:hasAssertion
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_assertion
;
np:hasProvenance
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_provenance
;
np:hasPublicationInfo
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_assertion
a
np:Assertion
.
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_provenance
a
np:Provenance
.
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_assertion
{
miriam-gene:3908
a
ncit:C16612
.
lld:C0699743
a
ncit:C7057
.
dgn-gda:DGN76ccd148277d60502d21376f12d10391
sio:SIO_000628
miriam-gene:3908
,
lld:C0699743
;
a
sio:SIO_001121
.
}
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_provenance
{
dgn-np:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_assertion
dcterms:description
"[Motor and sensory nerve conduction velocities (NCVs) and needle electromyography (EMG) results were reviewed in 26 children with different types of congenital muscular dystrophy (CMD), including patients with mutations in the genes LAMA2, FKRP, and COL6A2.]. 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:14755496
;
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:NP430251.RA2zdvtQM9iVYL7AdWrl1Uw9oFYjRoSQ13ceWzfEJ8EME130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:00+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" .
}