@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s
> .
@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:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_head
{
this:
np:hasAssertion
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion
;
np:hasProvenance
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance
;
np:hasPublicationInfo
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion
a
np:Assertion
.
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance
a
np:Provenance
.
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion
{
miriam-gene:5981
a
ncit:C16612
.
lld:C3495426
a
ncit:C7057
.
dgn-gda:DGN8a1fd1850f957e975f490fd61a207467
sio:SIO_000628
miriam-gene:5981
,
lld:C3495426
;
a
sio:SIO_001121
.
}
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_provenance
{
dgn-np:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_assertion
dcterms:description
"[The purposes of this study were to explore whether hyperhomocysteinemia was related to MTX administration and toxicity and whether homocysteine or MTX toxicity differed by methylenetetrahydrofolate reductase (MTHFR) or reduced folate carrier (RFC) genetic polymorphisms.]. 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:12915598
;
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:NP765820.RAIikyHnK6VLM3giasmEVQiEdgR_Q4b9mkYGImfCxlE7s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:43+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" .
}