@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY
> .
@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:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_head
{
this:
np:hasAssertion
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion
;
np:hasProvenance
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance
;
np:hasPublicationInfo
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion
a
np:Assertion
.
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance
a
np:Provenance
.
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN3a7d37e41a6ccd29c197aaa3bab190e2
sio:SIO_000628
miriam-gene:2153
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_provenance
{
dgn-np:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_assertion
dcterms:description
"[There were no significant differences in terms of diabetes mellitus, hypertension, dyslipidemia, plasma fibrinogen level, smoking, gender and family history of CAD with and without the FVL mutation in the patient group.]. 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:17982311
;
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:NP785914.RAXl4Wbyl7IzivBrwOC-LHiKM5efPZaJs08Ji7W8Sd4DY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}