@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA
> .
@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:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_head
{
this:
np:hasAssertion
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion
;
np:hasProvenance
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance
;
np:hasPublicationInfo
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion
a
np:Assertion
.
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance
a
np:Provenance
.
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0023462
a
ncit:C7057
.
dgn-gda:DGN27bd1e2ea7d4acf100b0246ab7a9f353
sio:SIO_000628
miriam-gene:2623
,
lld:C0023462
;
a
sio:SIO_001121
.
}
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_provenance
{
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_assertion
dcterms:description
"[These data show GATA1 mutations occur in utero in most DS TMD and AMKL, that they may occur without clinical signs of disease, and that multiple separate GATA1 mutant clones can occur in an individual.]. 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:14656875
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
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 .
}
dgn-np:NP423424.RAJ7Fepm0a8_un82sdwUzV7ibfdYtEdDeMusE6o410gPA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:57+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}