@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU
> .
@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:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_head
{
this:
np:hasAssertion
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_assertion
;
np:hasProvenance
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_assertion
a
np:Assertion
.
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_provenance
a
np:Provenance
.
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0152021
a
ncit:C7057
.
dgn-gda:DGN45d3d045ac5bfb4212412d6ea885a031
sio:SIO_000628
miriam-gene:4524
,
lld:C0152021
;
a
sio:SIO_001121
.
}
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_provenance
{
dgn-np:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_assertion
dcterms:description
"[To investigate the association of combined MTHFR C677T and A1298C gene polymorphisms with congenital heart diseases (CHD) in Egyptian children and their mothers and to determine their effect on homocysteine level in these children.]. 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:23933414
;
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:NP661839.RA2Yd_Ro2EH5O56uslmWDn8kXWdqcaJsUJ4xgw78hDoFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}