@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs
> .
@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:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_head
{
this:
np:hasAssertion
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_assertion
;
np:hasProvenance
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_provenance
;
np:hasPublicationInfo
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_assertion
a
np:Assertion
.
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_provenance
a
np:Provenance
.
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGN10106d972e80ab9a5c0a267cd999bb1d
sio:SIO_000628
miriam-gene:4524
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_provenance
{
dgn-np:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_assertion
dcterms:description
"[The purpose of this study was twofold: (1) to evaluate the putative association of MTHFR C677T and epithelial squamous cell carcinoma (ESCC) in Pakistan, and (2) to investigate whether de novo MTHFR C677T mutations are involved in the determination of ESCC phenotypes.]. 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:15583437
;
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:NP251971.RAdvln51IDnQ3quhFOB-TZ_Mmv8aywsdcIhhEiSDRrhEs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}