@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4
> .
@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:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_head
{
this:
np:hasAssertion
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_assertion
;
np:hasProvenance
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_assertion
a
np:Assertion
.
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_provenance
a
np:Provenance
.
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_assertion
{
miriam-gene:5340
a
ncit:C16612
.
lld:C0149871
a
ncit:C7057
.
dgn-gda:DGN9e95ea4c31f8b3d8d51faf746974446b
sio:SIO_000628
miriam-gene:5340
,
lld:C0149871
;
a
sio:SIO_001121
.
}
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_provenance
{
dgn-np:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_assertion
dcterms:description
"[In this study, we measured the plasminogen activity in patients with deep vein thrombosis and analyzed the DNA sequence to detect three point mutations (Ala601Thr, Val355Phe and Asp676Asn) in patients with hypo/dysplasminogenemia.]. 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:12692411
;
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:NP330395.RAs5L3RoV3kNiSPRz08j9U9xvoKKJMZm7hbCsUZX9kKS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}