@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw
> .
@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:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_head
{
this:
np:hasAssertion
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion
;
np:hasProvenance
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion
a
np:Assertion
.
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance
a
np:Provenance
.
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNf4ef335efb2cb6af154e67a2e1a33fd5
sio:SIO_000628
miriam-gene:324
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_provenance
{
dgn-np:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_assertion
dcterms:description
"[In addition to polymorphic analysis, we have also searched germline mutations of the APC gene in eight individuals (26 percent of all 31 at risk persons) of another two FAP families which could not be diagnosed definitely by linkage analysis.]. 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:7913010
;
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:NP1326401.RAtACj-xcxHNwkOYw4AbzLNcsmTDpmdRQ42b0lttPsmCw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:47+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" .
}