@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI
> .
@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:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_head
{
this:
np:hasAssertion
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_assertion
;
np:hasProvenance
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_provenance
;
np:hasPublicationInfo
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_assertion
a
np:Assertion
.
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_provenance
a
np:Provenance
.
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_assertion
{
miriam-gene:2160
a
ncit:C16612
.
lld:C0005779
a
ncit:C7057
.
dgn-gda:DGN0e2a88ed3aed9a2f706c2e589227ff41
sio:SIO_000628
miriam-gene:2160
,
lld:C0005779
;
a
sio:SIO_001121
.
}
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_provenance
{
dgn-np:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_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:NP284060.RAgFT4eY30kuZdIJ2u2EtJUPUj0SdrMRVKc9hu2CvD1BI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}