@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4
> .
@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:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_head
{
this:
np:hasAssertion
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_assertion
;
np:hasProvenance
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_provenance
;
np:hasPublicationInfo
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_assertion
a
np:Assertion
.
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_provenance
a
np:Provenance
.
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_assertion
{
miriam-gene:4709
a
ncit:C16612
.
lld:C0040038
a
ncit:C7057
.
dgn-gda:DGN7c497eca3b34da9fd6c3612f6148c961
sio:SIO_000628
miriam-gene:4709
,
lld:C0040038
;
a
sio:SIO_001121
.
}
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_provenance
{
dgn-np:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_assertion
dcterms:description
"[Therefore, we evaluated plasma total homocysteine (tHcy), folate, and vitamin B12 levels and established, by polymerase chain reaction, the presence of the C677T mutation (A223V) in the methylenetetrahydrofolate reductase (MTHFR) gene in 220 cases with VTE without well-established prothrombotic defects.]. 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:10397696
;
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:NP804843.RAxv98O75WULgb5Y40aCgqUh-hWDg14MfTzgq0VN9WEa4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+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" .
}