@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc
> .
@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:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_head
{
this:
np:hasAssertion
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_assertion
;
np:hasProvenance
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_provenance
;
np:hasPublicationInfo
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_assertion
a
np:Assertion
.
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_provenance
a
np:Provenance
.
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGNcdc092d8494a8e622ddbf2b18ace9aab
sio:SIO_000628
miriam-gene:5624
,
lld:C0007115
;
a
sio:SIO_001121
.
}
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_provenance
{
dgn-np:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_assertion
dcterms:description
"[We report novel APC mutations and present two FAP cases that suggest familial aggregation of thyroid cancer and demonstrate the need to consider attenuated FAP also among elderly patients with colon cancer.]. 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:19036155
;
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:NP276481.RALeADHh_W8MQV5Y9bxEdSsrA2RVuJaIeg5mRHC_Xpxrc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}