@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_head
{
this:
np:hasAssertion
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_assertion
;
np:hasProvenance
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_assertion
a
np:Assertion
.
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_provenance
a
np:Provenance
.
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1883486
a
ncit:C7057
.
dgn-gda:DGNcf9ec13edfc17245e96e651d7d699337
sio:SIO_000628
miriam-gene:4436
,
lld:C1883486
;
a
sio:SIO_001122
.
}
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_provenance
{
dgn-np:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_assertion
dcterms:description
"[Genetic counseling and testing for the MSH2 A636P mutation is indicated for Ashkenazi Jewish women with an endometrial cancer, especially if the cancer is detected before the age of 70 years in women with a personal or family history of colorectal cancer.]. 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:18674656
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP685609.RAp7KxYgITzOgxzc8995k5D2be3uzVULwy8rPFzl9gKZs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:56+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}