@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0
> .
@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:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_head
{
this:
np:hasAssertion
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_assertion
;
np:hasProvenance
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_assertion
a
np:Assertion
.
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_provenance
a
np:Provenance
.
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_assertion
{
miriam-gene:28
a
ncit:C16612
.
lld:C0042974
a
ncit:C7057
.
dgn-gda:DGN28e2353a5a49a4b9b4e36c2d4ac3e647
sio:SIO_000628
miriam-gene:28
,
lld:C0042974
;
a
sio:SIO_001121
.
}
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_provenance
{
dgn-np:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_assertion
dcterms:description
"[It was the objective of the present study to evaluate the distribution of VWF levels in young females with or without bleeding symptoms in this population, and the influence of ABO blood group and promoter haplotypes on VWF levels and to identify a possible increased prevalence of VWD in females with bleeding symptoms.]. 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:18521502
;
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:NP795569.RAn1IAMBvLDBU20yGbbCylCbflZ6RQJFw3c4dTix7Mp_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}