@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0
> .
@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:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_head
{
this:
np:hasAssertion
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_assertion
;
np:hasProvenance
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_provenance
;
np:hasPublicationInfo
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_assertion
a
np:Assertion
.
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_provenance
a
np:Provenance
.
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNbffb2f11e537bd02d22f0c109aa8fdb8
sio:SIO_000628
miriam-gene:324
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_provenance
{
dgn-np:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_assertion
dcterms:description
"[Many cases of HNPCC are due to germline mutations in DNA mismatch repair genes, leading to the tumor phenotype of microsatellite instability (MSI), and most cases of FAP are caused by germline APC mutations.]. 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:11135435
;
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:NP304175.RAZRXIJ7W5HNzww7Ercx_qzXP7NXMZklSQWTJYmOFWsE0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:03+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" .
}