@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M
> .
@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:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_head
{
this:
np:hasAssertion
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion
;
np:hasProvenance
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance
;
np:hasPublicationInfo
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion
a
np:Assertion
.
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance
a
np:Provenance
.
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion
{
miriam-gene:6442
a
ncit:C16612
.
lld:C0410173
a
ncit:C7057
.
dgn-gda:DGN2dac36fe2d21ca539f534dbe12d38f15
sio:SIO_000628
miriam-gene:6442
,
lld:C0410173
;
a
sio:SIO_001121
.
}
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_provenance
{
dgn-np:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_assertion
dcterms:description
"[It has been previously shown in Tunisian and Algerian families that the locus for SCARMD maps to the proximal part of 13q, and in Algerian families that the disease is associated with deficiency of the 50 kDa dystrophin associated glycoprotein (50DAG).]. 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:8071965
;
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:NP429570.RASvE-IPgrM7iwUHlHKxAk62i4wiEP9JuT3UWIcbgaE7M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}