@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8
> .
@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:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_head
{
this:
np:hasAssertion
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_assertion
;
np:hasProvenance
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_provenance
;
np:hasPublicationInfo
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_assertion
a
np:Assertion
.
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_provenance
a
np:Provenance
.
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNa1d55ffc05e944f4a881ede821f6b7fa
sio:SIO_000628
miriam-gene:4524
,
lld:C0007097
;
a
sio:SIO_001122
.
}
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_provenance
{
dgn-np:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_assertion
dcterms:description
"[Data indicate the C677T MTHFR polymorphism does not significantly contribute to the genetic susceptibility to breast and prostate cancer, while show some evidence for possible genetic contribution to the development of head and neck carcinoma.]. 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:17573062
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP100423.RAVpx0b6S_p0SdrXXwZFHiXb_TmWeEINAnfpoSJ0f4oS8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:51+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" .
}