@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco
> .
@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:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_head
{
this:
np:hasAssertion
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_assertion
;
np:hasProvenance
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_provenance
;
np:hasPublicationInfo
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_assertion
a
np:Assertion
.
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_provenance
a
np:Provenance
.
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGN934c7e547c3903bf90d8410bea4e1d5b
sio:SIO_000628
miriam-gene:8170
,
lld:C0002895
;
a
sio:SIO_001121
.
}
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_provenance
{
dgn-np:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_assertion
dcterms:description
"[The C677T methylenetetrahydrofolate reductase (MTHFR) gene polymorphism and the G20210A mutation at the 3' untranslated region (3'UTR) of the prothrombin gene may be considered to be genetic risk factors that contribute to the clinical heterogeneity in sickle cell disease.]. 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:15481892
;
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:NP331603.RArjdflSqMS-uzT--VZkaq8EKNb3k_1r03wS_la0TfAco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:15+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" .
}