@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY
> .
@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:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_head
{
this:
np:hasAssertion
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_assertion
;
np:hasProvenance
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_assertion
a
np:Assertion
.
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_provenance
a
np:Provenance
.
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_assertion
{
miriam-gene:2155
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNeaeb82006d99d8a41e209b75377f1fcc
sio:SIO_000628
miriam-gene:2155
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_provenance
{
dgn-np:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_assertion
dcterms:description
"[Since there is evidence that FVII levels constitute a risk factor for coronary heart disease and considering the importance of F7 DNA polymorphisms in determining FVII levels, further analyses of these polymorphisms should yield information to aid the understanding of the quantitative variation in FVII levels and the relative genetic risk for cardiovascular disease in the general population.]. 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:12935978
;
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:NP249694.RALYkRNsoNvp1EvvTFK_y_OUoCk5tfwVS7A2UvWaFeXvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}