@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY
> .
@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:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_head
{
this:
np:hasAssertion
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion
;
np:hasProvenance
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance
;
np:hasPublicationInfo
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion
a
np:Assertion
.
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance
a
np:Provenance
.
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion
{
miriam-gene:7871
a
ncit:C16612
.
lld:C0023269
a
ncit:C7057
.
dgn-gda:DGNc4f724d24ce4b12f95cda9ff445444d1
sio:SIO_000628
miriam-gene:7871
,
lld:C0023269
;
a
sio:SIO_001121
.
}
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_provenance
{
dgn-np:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_assertion
dcterms:description
"[Group 1 comprises approximately 25% of all LMSs, and is defined by a shared pattern of gene expression, a distinct pattern of genomic changes, and reactivity for at least 3 of 5 immunohistochemistry (IHC) markers (smooth muscle gamma actin, calsequestrin 2, human muscle cofilin2, myosin light chain kinase, and sarcolemmal membrane associated protein), as tested on 271 cases of LMS in tissue microarrays.]. 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:21412072
;
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:NP370387.RArxCbsDFASSJGc3Xsnvs_bYCthAmJYfRstK0lL6T1cLY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}