@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw
> .
@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:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_head
{
this:
np:hasAssertion
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion
;
np:hasProvenance
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion
a
np:Assertion
.
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance
a
np:Provenance
.
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0272375
a
ncit:C7057
.
dgn-gda:DGN8c4b8a7123aa4f9ac7b762f9873a4d6c
sio:SIO_000628
miriam-gene:5660
,
lld:C0272375
;
a
sio:SIO_001121
.
}
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_provenance
{
dgn-np:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_assertion
dcterms:description
"[In addition, inherited prothrombotic defects, such as protein C, protein S, and antithrombin deficiencies, and genetic mutations for FV Leiden, prothrombin gene G20210A (FII G20210A), and methyltetrahydrofolate reductase C677T (MTHFR C677T) were studied.]. 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:22048515
;
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:NP215526.RA5Lknu4hrxVCl7FW0_TqBJFv3R5MImbhCLJ9I4q_QgUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}