@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M
> .
@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:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_head
{
this:
np:hasAssertion
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_assertion
;
np:hasProvenance
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_provenance
;
np:hasPublicationInfo
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_assertion
a
np:Assertion
.
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_provenance
a
np:Provenance
.
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGNeab99869164a943d6594f3d03cf581f2
sio:SIO_000628
miriam-gene:4524
,
lld:C0021364
;
a
sio:SIO_001121
.
}
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_provenance
{
dgn-np:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_assertion
dcterms:description
"[The C677T polymorphism (rs1801133) of the MTHFR gene affects the MTHFR activity, modifies the homocysteine plasma concentration and, among others, increases the risks for idiopathic male infertility, including erectile dysfunction (ED).]. 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:23090267
;
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:NP434013.RAzj0QOvXpyvnPcyx34S_KSS2XmAwBFS25IcLBK2oe20M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}