@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk
> .
@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:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_head
{
this:
np:hasAssertion
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_assertion
;
np:hasProvenance
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_assertion
a
np:Assertion
.
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_provenance
a
np:Provenance
.
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGNa63a98c6b9ce0061491d1d0a41aac2b8
sio:SIO_000628
miriam-gene:324
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_provenance
{
dgn-np:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_assertion
dcterms:description
"[Molecular genetics has identified some inherited mutations (such as at APC and the mismatch repair loci) that predispose to colon cancer and some somatic mutations (such as at APC and p53) that cause sporadic colon tumours.]. 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:9156280
;
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:NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}