@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY
> .
@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/v3.0.0/void/
> .
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_head
{
this:
np:hasAssertion
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_assertion
;
np:hasProvenance
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_provenance
;
np:hasPublicationInfo
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_assertion
a
np:Assertion
.
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_provenance
a
np:Provenance
.
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_assertion
{
miriam-gene:4633
a
ncit:C16612
.
lld:C0949658
a
ncit:C7057
.
dgn-gda:DGN47be1139db48d1ef9011517bf9624a8e
sio:SIO_000628
miriam-gene:4633
,
lld:C0949658
;
a
sio:SIO_001121
.
}
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_provenance
{
dgn-np:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_assertion
dcterms:description
"[In conclusion, we show that mutations in the MYL2 gene may be involved in familial and classical forms of hypertrophic cardiomyopathy, and we provide new tools for the genetic analysis of patients with familial hypertrophic cardiomyopathy.]. 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:9535554
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP583851.RASRYk8nW04BiqPA6s_Kp3eU5cT4DengfUPwX89IGB0cY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:29+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}