@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4
> .
@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:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_head
{
this:
np:hasAssertion
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion
;
np:hasProvenance
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance
;
np:hasPublicationInfo
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion
a
np:Assertion
.
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance
a
np:Provenance
.
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025267
a
ncit:C7057
.
dgn-gda:DGNeaa8ae73b2e8dbee109b67356ce5c9a8
sio:SIO_000628
miriam-gene:5979
,
lld:C0025267
;
a
sio:SIO_001121
.
}
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_provenance
{
dgn-np:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_assertion
dcterms:description
"[MEN1 gene mutation and RET codon 791 mutation in the same patient did not affect the typical phenotype of MEN1 or MEN2, and also the course of diseases seems to be unchanged.]. 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:15870131
;
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:NP874107.RA5Wm4hzWHWFPYiUemUMCBaR9KxS8DAjGt-xdRYrdYkX4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}