@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw
> .
@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:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_head
{
this:
np:hasAssertion
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_assertion
;
np:hasProvenance
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_assertion
a
np:Assertion
.
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_provenance
a
np:Provenance
.
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN19871f61d529b08fbbc40569da370531
sio:SIO_000628
miriam-gene:4436
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_provenance
{
dgn-np:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_assertion
dcterms:description
"[In the United States, it was recently reported that the prevalence of Lynch syndrome with an hMSH2 mutation in patients with endometrial cancer in the lower uterine segment (LUS) is much greater than that in patients with endometrial cancer, although no such reports have been published in Asia.]. 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:22940821
;
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:NP1009717.RAk4mTb1p4tH0ObHNzFwQ27hXvKrpEkqFFizxRYpbEGpw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:23+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" .
}