@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc
> .
@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:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_head
{
this:
np:hasAssertion
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_assertion
;
np:hasProvenance
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_provenance
;
np:hasPublicationInfo
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_assertion
a
np:Assertion
.
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_provenance
a
np:Provenance
.
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_assertion
{
miriam-gene:4625
a
ncit:C16612
.
lld:C0949658
a
ncit:C7057
.
dgn-gda:DGN9a7c6877b50a49182fea016357cae8fa
sio:SIO_000628
miriam-gene:4625
,
lld:C0949658
;
a
sio:SIO_001121
.
}
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_provenance
{
dgn-np:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_assertion
dcterms:description
"[We studied 82 probands with HCM in whom no mutations had been found in MYH7 exons encoding the head and neck regions of myosin nor in the other frequently implicated disease genes.]. 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:11861413
;
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:NP215035.RAhw45rvRPlv_VcTNgGqhtYPkFMpgVGB9ZToZtaxDr9tc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}