@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o
> .
@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/v4.0.0/void/
> .
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_head
{
this:
np:hasAssertion
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_provenance
a
np:Provenance
.
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4656
a
ncit:C16612
.
lld:C0035412
a
ncit:C7057
.
dgn-gda:DGN7b8677813a6b2f24da7f601b975a90fc
sio:SIO_000628
miriam-gene:4656
,
lld:C0035412
;
a
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.
}
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_provenance
{
dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_assertion
dcterms:description
"[These four cases are essentially identical to the three unusual RMSs recently reported by Mentzel and Katenkamp as sclerosing, pseudovascular rhabdomyosarcoma in adults. Although the focal alveolar architecture and the primitive cytologic appearance of these hyalinizing RMS suggest a relationship with ARMS, the presence of abundant strap cells in one case, the predominant expression of MyoD1 rather than myogenin, and the absence of ARMS-associated fusions genes point more strongly toward a variant of ERMS.]. 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:12218574
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP367405.RAsyyHowGSdn_iiaZhNUMgiJU6v2ESE57BBT6DC4PlG3o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:32+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
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;
pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
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<
http://orcid.org/0000-0003-0169-8159
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pav:version
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"v4.0.0" .
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