@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA
> .
@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:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_head
{
this:
np:hasAssertion
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_assertion
;
np:hasProvenance
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_provenance
;
np:hasPublicationInfo
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_assertion
a
np:Assertion
.
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_provenance
a
np:Provenance
.
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0003469
a
ncit:C7057
.
dgn-gda:DGNd75f3928c97bf394c445d4742392a8c0
sio:SIO_000628
miriam-gene:5624
,
lld:C0003469
;
a
sio:SIO_001121
.
}
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_provenance
{
dgn-np:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_assertion
dcterms:description
"[Reasons offered for maintaining surveillance included the need for additional confirmation of the APC mutation in two affected relatives, the possibility of sampling error or two different mutations in an affected family, limited prospective data, and patient anxiety.]. 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:10223748
;
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:NP909095.RAWbWfRW8ujUXPGGB6jWjjUrjlrs2U_zVguQX9MKzf8KA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:18+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" .
}