@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs
> .
@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:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_head
{
this:
np:hasAssertion
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_assertion
;
np:hasProvenance
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_provenance
;
np:hasPublicationInfo
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_assertion
a
np:Assertion
.
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_provenance
a
np:Provenance
.
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_assertion
{
miriam-gene:3053
a
ncit:C16612
.
lld:C2827470
a
ncit:C7057
.
dgn-gda:DGNfd37baf4c2a60fcf996a2edfd79dfcda
sio:SIO_000628
miriam-gene:3053
,
lld:C2827470
;
a
sio:SIO_001121
.
}
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_provenance
{
dgn-np:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_assertion
dcterms:description
"[Other causes of inherited thrombophilia include hyperhomocysteinemia, abnormalities in the proteins of the fibrinolytic system, dysfibrinogenemias, deficiency of heparin cofactor II, abnormal thrombomodulin, and the recently described variation in the prothrombin gene.]. 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:9840687
;
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:NP824500.RAiGKK5oljbv352fRDCPWWRDLL5jlLAir-U_oZOHXNhqs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}