@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI
> .
@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/v3.0.0/void/
> .
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_head
{
this:
np:hasAssertion
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion
;
np:hasProvenance
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance
;
np:hasPublicationInfo
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion
a
np:Assertion
.
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance
a
np:Provenance
.
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN70747abf6b5da30f7a48729b8167516b
sio:SIO_000628
miriam-gene:4360
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_provenance
{
dgn-np:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_assertion
dcterms:description
"[Deleterious germ-line variants involving the DNA mismatch repair (MMR) genes have been identified as the cause of the hereditary nonpolyposis colorectal cancer syndrome known as the Lynch syndrome, but in numerous familial clusters of colon cancer, the cause remains obscure.]. 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:21671081
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP568451.RAThesqbAUiFiEwM8ujCrylV1j4Gftf94dWLP_QPxLYPI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:18+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}