@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno
> .
@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:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_head
{
this:
np:hasAssertion
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_assertion
;
np:hasProvenance
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_provenance
;
np:hasPublicationInfo
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_assertion
a
np:Assertion
.
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_provenance
a
np:Provenance
.
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_assertion
{
miriam-gene:5660
a
ncit:C16612
.
lld:C0259744
a
ncit:C7057
.
dgn-gda:DGN137ee55efbe11fd3a4c30dc9e8aea17a
sio:SIO_000628
miriam-gene:5660
,
lld:C0259744
;
a
sio:SIO_001121
.
}
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_provenance
{
dgn-np:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_assertion
dcterms:description
"[The dose of warfarin required to maintain the prothrombin time in a range of 1.8 to 2.2 times normal varied considerably during short periods, a phenomenon that may have been due to several factors: hypercatabolism of the drug with prolonged administration, abnormality of liver function, variation in levels of serum albumin, fluctuations in drug dosage secondary to oral administration, and variations in dietary vitamin K. Protein C determinations by immunologic and functional assays consistently showed detectable but reduced protein C antigen levels with undetectable activity levels, suggesting that a dysproteinemia rather than a deficiency of synthesis is responsible for the child's coagulopathy.]. 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:3340476
;
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:NP746479.RABd_SJ1h4ziJadV4MFeeKQiyt_H4SfYZ3tbDJ3CtxEno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+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" .
}