@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4
> .
@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:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_head
{
this:
np:hasAssertion
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_assertion
;
np:hasProvenance
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_provenance
;
np:hasPublicationInfo
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_assertion
a
np:Assertion
.
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_provenance
a
np:Provenance
.
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_assertion
{
miriam-gene:79612
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNb6b3c970fbcdfd7290f4af7941d12572
sio:SIO_000628
miriam-gene:79612
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_provenance
{
dgn-np:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_assertion
dcterms:description
"[In this study, we determined the NAT2 genotype in members of one large FAP family and three smaller ones all of which had been shown to harbor the same germline APC gene mutation.]. 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:9156320
;
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:NP772735.RA5xRXuyJw-SuG_03gmlZGrQbcZWka0Pe4GGmC2TZGvU4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:47+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: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" .
}