@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag
> .
@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:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_head
{
this:
np:hasAssertion
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_assertion
;
np:hasProvenance
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_provenance
;
np:hasPublicationInfo
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_assertion
a
np:Assertion
.
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_provenance
a
np:Provenance
.
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN0b1f0d6460480c18a7485e402634524f
sio:SIO_000628
miriam-gene:5624
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_provenance
{
dgn-np:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_assertion
dcterms:description
"[Molecular testing directed at colorectal neoplasia is currently in use for diagnosis and characterization of rare, highly penetrant inherited syndromes due to germline mutation of the APC suppressor gene or DNA nucleotide mismatch repair genes.]. 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:10539901
;
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:NP343997.RAy80vYF3-EeLvodK4-bE1A-Y3hQrfa049sktw0cid3ag130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}