@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY
> .
@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:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_head
{
this:
np:hasAssertion
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_assertion
;
np:hasProvenance
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_provenance
;
np:hasPublicationInfo
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_assertion
a
np:Assertion
.
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_provenance
a
np:Provenance
.
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGNe5f1e18b3e198283bf21a2f4052acdc7
sio:SIO_000628
miriam-gene:4524
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_provenance
{
dgn-np:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_assertion
dcterms:description
"[A prospective study was conducted on men seeking care at the infertility clinic in Milano to determine if the MTHFR C677T polymorphism is associated with infertility, and if such an association is modified by a common deletion of one of the glutathione transferases, GSTM1.]. 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:16484136
;
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:NP324573.RAcXuLl7f93ukbW1mX2KTTWgN8I-4TIP9sxXOydd1z_iY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}