@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0
> .
@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:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_head
{
this:
np:hasAssertion
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_assertion
;
np:hasProvenance
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_assertion
a
np:Assertion
.
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_provenance
a
np:Provenance
.
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN354d50f4335045aa4620a75977faddf0
sio:SIO_000628
miriam-gene:7276
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_provenance
{
dgn-np:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_assertion
dcterms:description
"[We propose an approach to molecular diagnosis in European patients with FAP, apart from members of families with known mutations, based on the frequency of TTR mutations observed in this and and other studies of FAP in Europe.]. 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:7655883
;
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:NP1316704.RAjjB7cskDh9Zi9uq-6vIDpukH7ZVqyee41PzBzvzJVo0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:43+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" .
}