@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw
> .
@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 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:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_head
{
this:
np:hasAssertion
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion
;
np:hasProvenance
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance
;
np:hasPublicationInfo
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion
a
np:Assertion
.
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance
a
np:Provenance
.
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0042974
a
ncit:C7057
.
dgn-gda:DGN87d9f84c60679ae80f62929647e4f0e5
sio:SIO_000628
miriam-gene:7450
,
lld:C0042974
;
a
sio:SIO_001122
.
}
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_provenance
{
dgn-np:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_assertion
dct:description
"[In conclusion, the automated fluorescent capillary electrophoresis method presented here is an extremely rapid, simple and highly informative technique for association studies between VWD and the VWF gene in addition to genetic counseling and prenatal diagnosis by precise linkage analysis in VWD-affected families.]. 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:15886817
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59268.RA0xl6-3FLeh3KxuJaPP4EBaT6JuudWYJpDMFrMzfl7Dw130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}