@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k
> .
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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:
np:hasAssertion
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_assertion
a
np:Assertion
.
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_provenance
a
np:Provenance
.
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_assertion
{
miriam-gene:79971
a
ncit:C16612
.
lld:C0019069
a
ncit:C7057
.
dgn-gda:DGN3067b47ae9227ad51b16a24cc6bf4fad
sio:SIO_000628
miriam-gene:79971
,
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;
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.
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dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_provenance
{
dgn-np:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_assertion
dcterms:description
"[To establish a rapid and automatic gene analysis method, we used capillary electrophoresis (CE) for the analysis of the intron 13 microsatellite repeat polymorphism (MRP) of the coagulation factor VIII gene for the diagnosis of hemophilia A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:10805288
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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:NP780769.RADVWnChC-HSliCsYHkb3VrK4jdE91FXsFbqtYLNiP5-k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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