@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs
> .
@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:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_head
{
this:
np:hasAssertion
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_assertion
;
np:hasProvenance
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_provenance
;
np:hasPublicationInfo
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_assertion
a
np:Assertion
.
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_provenance
a
np:Provenance
.
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_assertion
{
miriam-gene:2191
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN3bf8b22873a53726e699a5ae4645286f
sio:SIO_000628
miriam-gene:2191
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_provenance
{
dgn-np:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_assertion
dcterms:description
"[Correlation between the molecular analysis and ophthalmic examinations, performed without knowledge of clinical and genetic status respectively, provided additional evidence in favour of the view that the range of phenotypic expression in FAP may result from different allelic manifestations of APC mutations.]. 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:8733048
;
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:NP1354550.RA2I6nhgSbfgmb-wBMFN1B17YidxJkHfdrMcO_EJDFETs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:00+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" .
}