@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI
> .
@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:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_head
{
this:
np:hasAssertion
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_assertion
;
np:hasProvenance
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_provenance
;
np:hasPublicationInfo
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_assertion
a
np:Assertion
.
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_provenance
a
np:Provenance
.
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN63cf6844d312f49970092f8b7f4c845b
sio:SIO_000628
miriam-gene:5624
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_provenance
{
dgn-np:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_assertion
dcterms:description
"[Mutations of the APC gene are thought to be responsible for the development of FAP, and the location of the mutation on the gene is thought to influence the nature of the extracolonic manifestations that a given patient might develop.]. 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:15592657
;
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:NP472423.RArj0S57GmC5cZT9p7rT1srR08GE7TgU2U1DFbDljZ0fI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:19+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" .
}