@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8
> .
@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:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_head
{
this:
np:hasAssertion
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_assertion
;
np:hasProvenance
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_assertion
a
np:Assertion
.
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_provenance
a
np:Provenance
.
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGNa11035edf5593288bb46927efe59f0de
sio:SIO_000628
miriam-gene:875
,
lld:C0598608
;
a
sio:SIO_001121
.
}
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_provenance
{
dgn-np:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_assertion
dcterms:description
"[To test this possibility, we studied cDNA derived from four well characterized patients with POAD, exhibiting hyperhomocysteinemia and reduced CBS activities, from four normal controls, and from four obligatory heterozygotes for CBS deficiency.]. 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:7633411
;
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:NP278245.RAaAr_wNouhhKUUS1O49nvxO63Qr-s7Y_BRuYhYmOxJV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}