@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s
> .
@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:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_head
{
this:
np:hasAssertion
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_assertion
;
np:hasProvenance
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_assertion
a
np:Assertion
.
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_provenance
a
np:Provenance
.
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN9f3973a732525a8cd6ad76ab87bfc4f5
sio:SIO_000628
miriam-gene:5781
,
lld:C0028326
;
a
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.
}
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_provenance
{
dgn-np:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_assertion
dcterms:description
"[We conclude that (a) most of our clinically diagnosed NS cases were sporadic (b) PTPN11 analysis should be limited to those fulfilling the relevant NS criteria (c) Cardiovascular evaluation should comprise all NS patients, while pulmonary stenosis, short stature, and thorax deformities prevailed among those with PTPN11 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:21590266
;
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:NP171044.RA68IlA4rvIiCgXPUWF1YRCn-a2Gg6c6X5s8nvB2Nt-5s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}