@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs
> .
@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:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_head
{
this:
np:hasAssertion
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_assertion
;
np:hasProvenance
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_provenance
;
np:hasPublicationInfo
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_assertion
a
np:Assertion
.
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_provenance
a
np:Provenance
.
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1336076
a
ncit:C7057
.
dgn-gda:DGNe15e420f1513d6a6836909e79c1093da
sio:SIO_000628
miriam-gene:4524
,
lld:C1336076
;
a
sio:SIO_001121
.
}
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_provenance
{
dgn-np:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_assertion
dcterms:description
"[The role of allele variants 677T and 1298C (MTHFR gene) and 2756G (MS gene) has been investigated as potentially modifying factors of BRCA gene penetrance, evaluated as age at first diagnosis of cancer, in 484 BRCA1/BRCA2 carriers and in 108 sporadic breast cancer cases as a control group.]. 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:17151928
;
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:NP721724.RA-k9o2TN7Za-TjYpzjMLDRJCiAaOvieIqjDVZ6f74cLs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}