@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8
> .
@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:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_head
{
this:
np:hasAssertion
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_assertion
;
np:hasProvenance
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_provenance
;
np:hasPublicationInfo
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_assertion
a
np:Assertion
.
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_provenance
a
np:Provenance
.
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_assertion
{
miriam-gene:7499
a
ncit:C16612
.
lld:C0917713
a
ncit:C7057
.
dgn-gda:DGN2c9c48aab16e5671587747a1f68db648
sio:SIO_000628
miriam-gene:7499
,
lld:C0917713
;
a
sio:SIO_001121
.
}
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_provenance
{
dgn-np:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_assertion
dcterms:description
"[Sixteen three generation families from the West of Scotland with Duchenne muscular dystrophy (DMD) or Becker muscular dystrophy (BMD) have been studied using the Xg blood group and seven cloned DNA sequences which recognise DNA polymorphisms on the short arm of the X chromosome (Xp).]. 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:3860471
;
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:NP458592.RAEn63fZhIB-Usqfy2I80exiiPwMJts1LWbafDNJfxvv8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}