@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw
> .
@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:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_head
{
this:
np:hasAssertion
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_assertion
;
np:hasProvenance
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_provenance
;
np:hasPublicationInfo
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_assertion
a
np:Assertion
.
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_provenance
a
np:Provenance
.
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_assertion
{
miriam-gene:2160
a
ncit:C16612
.
lld:C0019087
a
ncit:C7057
.
dgn-gda:DGNe1708b7206b277f7b9d1c70ccef1e22f
sio:SIO_000628
miriam-gene:2160
,
lld:C0019087
;
a
sio:SIO_001121
.
}
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_provenance
{
dgn-np:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_assertion
dcterms:description
"[A deficiency of FXI is an unusual hemorrhagic diathesis in that the bleeding tendency can be highly variable, ranging from severe deficiencies with no symptoms to mild and moderate deficiencies requiring multiple blood transfusions for hemorrhages.]. 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:15456480
;
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:NP685883.RAq7iQTqwKOtTIIOFcasepo0PUuLcQKqtR1UnU1KDIyGw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}