@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U
> .
@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:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_head
{
this:
np:hasAssertion
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_assertion
;
np:hasProvenance
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_assertion
a
np:Assertion
.
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_provenance
a
np:Provenance
.
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN41ff8db069395082f1b05b690e159a22
sio:SIO_000628
miriam-gene:5624
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_provenance
{
dgn-np:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_assertion
dcterms:description
"[AXIN2 and MUTYH genes were screened for germline mutations by PCR and direct sequencing in 39 unrelated patients with multiple adenomas or colorectal cancer without evidence of APC mutation nor mismatch repair defect.]. 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:16941501
;
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:NP179723.RAdjT58bs3Hflc7a21nBYxljsKnFBS1Q0aEX7AhWZYS6U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}