@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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{
this:
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dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_provenance
a
np:Provenance
.
dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7499
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN24c8d6fa5db29d949cd7c26f1eb2a3e6
sio:SIO_000628
miriam-gene:7499
,
lld:C0026850
;
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.
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{
dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_assertion
dcterms:description
"[Analyses of 11 families with DMD and ten with BMD, informative for the Xg blood group, reinforce the conclusions of others that there is no measurable linkage between the loci for Xg and for the X-linked forms of muscular dystrophy.]. 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:6317539
;
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 .
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dgn-np:NP939241.RAJUrLNxUBaNDbjXO_Nf9MW4DCJEv2B-EhVSJTO2L2rvU130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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<
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> , <
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> , <
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> ;
pav:createdBy
<
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