@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA
> .
@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:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_head
{
this:
np:hasAssertion
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_assertion
;
np:hasProvenance
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_assertion
a
np:Assertion
.
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_provenance
a
np:Provenance
.
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGN683a17978a975309ce56e363b8800486
sio:SIO_000628
miriam-gene:5781
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_provenance
{
dgn-np:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_assertion
dcterms:description
"[In order to determine possible involvement of this gene in the pathogenesis of HCM, we performed mutation screening of the PTPN11 coding region in 250 selected HCM probands (200 patients without mutations in sarcomeric genes and 50 with identified 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:16488201
;
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:NP179089.RAl_vbw759jVuS82vOAJTG4UTz_ers4KViY84glx0iYFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}