@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4
> .
@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:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_head
{
this:
np:hasAssertion
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_assertion
;
np:hasProvenance
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_provenance
;
np:hasPublicationInfo
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_assertion
a
np:Assertion
.
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_provenance
a
np:Provenance
.
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0017097
a
ncit:C7057
.
dgn-gda:DGNb3df9cb8b7cf729a33371a929b33a859
sio:SIO_000628
miriam-gene:324
,
lld:C0017097
;
a
sio:SIO_001121
.
}
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_provenance
{
dgn-np:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_assertion
dcterms:description
"[The APC gene has been found to be altered by point mutations in the germ line of both adenomatous polyposis coli and Gardner's syndrome patients and somatically in tumors from sporadic colorectal cancer patients.]. 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:1324739
;
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:NP268177.RAF7BhgBXRsGZQefudDjhr0O6Ed33iQMJLvJmwmTq76A4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}