@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg
> .
@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:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_head
{
this:
np:hasAssertion
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_assertion
;
np:hasProvenance
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_provenance
;
np:hasPublicationInfo
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_assertion
a
np:Assertion
.
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_provenance
a
np:Provenance
.
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_assertion
{
miriam-gene:5554
a
ncit:C16612
.
lld:C0005779
a
ncit:C7057
.
dgn-gda:DGNbb6f9adf084f7606e898dcdc5846a66e
sio:SIO_000628
miriam-gene:5554
,
lld:C0005779
;
a
sio:SIO_001121
.
}
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_provenance
{
dgn-np:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_assertion
dcterms:description
"[None of the 21 patients had hereditary deficiencies of antithrombin III, protein C, or protein S. Our results indicate that the milder bleeding diathesis that is occasionally seen among Italian hemophiliacs with factor levels that are less than 1 percent cannot be explained by the concomitant expression of a known prothrombotic defect.]. 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:8607105
;
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:NP470123.RAo_bUIPomePsEQGa7pimmbg8b95_aLIcdY0mCLT0JgUg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}