@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ
> .
@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:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_head
{
this:
np:hasAssertion
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_assertion
;
np:hasProvenance
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_assertion
a
np:Assertion
.
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_provenance
a
np:Provenance
.
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_assertion
{
miriam-gene:4363
a
ncit:C16612
.
lld:C0019069
a
ncit:C7057
.
dgn-gda:DGNda11f42fc29e94547d0d90052d33e67c
sio:SIO_000628
miriam-gene:4363
,
lld:C0019069
;
a
sio:SIO_001121
.
}
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_provenance
{
dgn-np:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_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
;
sio:SIO_000772
miriam-pubmed:10805288
;
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:NP182891.RAL1p0MMYPyJDVqi5Ibk3VicvtgflNg5Xll1rmBHB6qoQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}