@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0
> .
@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:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_head
{
this:
np:hasAssertion
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_assertion
;
np:hasProvenance
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_assertion
a
np:Assertion
.
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_provenance
a
np:Provenance
.
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_assertion
{
miriam-gene:2147
a
ncit:C16612
.
lld:C2584620
a
ncit:C7057
.
dgn-gda:DGN01bfef317223eeaab9b5f067ae23455e
sio:SIO_000628
miriam-gene:2147
,
lld:C2584620
;
a
sio:SIO_001121
.
}
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_provenance
{
dgn-np:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_assertion
dcterms:description
"[The most common causes of hereditary thrombophilia are reviewed with an emphasis on resistance to activated protein C, prothrombin variant 20210A, and hyperhomocystinemia, and the current status of laboratory testing for thrombophilia is discussed.]. 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:9817680
;
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:NP353259.RAtRMwa9Qg08etulN1ox5oSRqofgEnpWNP5OFa6hLjQx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}