@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8
> .
@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:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_head
{
this:
np:hasAssertion
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_assertion
;
np:hasProvenance
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_provenance
;
np:hasPublicationInfo
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_assertion
a
np:Assertion
.
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_provenance
a
np:Provenance
.
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN1badedf694412b11e7ce090086d9a254
sio:SIO_000628
miriam-gene:4595
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_provenance
{
dgn-np:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_assertion
dcterms:description
"[Together, our results indicate that heterozygous MUTYH mutations are associated with families that include both breast cancer patients and colorectal cancer patients, independent of which tumour type is more prevalent in the family.]. 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:20191381
;
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:NP715567.RAohgCN369n2jIB8fl00gZfKUYuhabNSEsLlCb10Fmtt8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}