@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU
> .
@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:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_head
{
this:
np:hasAssertion
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_assertion
;
np:hasProvenance
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_provenance
;
np:hasPublicationInfo
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_assertion
a
np:Assertion
.
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_provenance
a
np:Provenance
.
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_assertion
{
miriam-gene:7450
a
ncit:C16612
.
lld:C0085411
a
ncit:C7057
.
dgn-gda:DGN580f92a3c1333583a2e03873e1a6b427
sio:SIO_000628
miriam-gene:7450
,
lld:C0085411
;
a
sio:SIO_001121
.
}
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_provenance
{
dgn-np:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_assertion
dcterms:description
"[The association between bleeding disorders and pulmonary angiodysplasia has rarely presented in literature and deficiency of von Willebrand factor might increase the risk of bleeding in patients with coexisting angiodysplastic disease.]. 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:9066252
;
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:NP382263.RAL3HPCuW3WVkfnohZ8ytdvMUoo-M0ssn92iWe-JGVGAU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}