@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg
> .
@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:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_head
{
this:
np:hasAssertion
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion
;
np:hasProvenance
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance
;
np:hasPublicationInfo
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion
a
np:Assertion
.
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance
a
np:Provenance
.
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0242666
a
ncit:C7057
.
dgn-gda:DGNce44d181f23f906ba150d298ba460eba
sio:SIO_000628
miriam-gene:5660
,
lld:C0242666
;
a
sio:SIO_001121
.
}
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_provenance
{
dgn-np:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_assertion
dcterms:description
"[Although these traits are present at relatively high prevalence in the population, the magnitude of the increased thrombotic risk associated with these factors is substantially less than that related to inherited deficiency of the natural anticoagulant protein antithrombin, and somewhat less than the elevated risk with protein C and protein S deficiencies.]. 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:11286642
;
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:NP177327.RAWVX791ZksJF9a_dye5RGPhPs8FQ92vWeD_PEaUWDSMg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}