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http://rdf.disgenet.org/nanopublications.trig#NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI
> .
@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:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_head
{
this:
np:hasAssertion
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion
a
np:Assertion
.
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_provenance
a
np:Provenance
.
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion
{
miriam-gene:3047
a
ncit:C16612
.
lld:C1868112
a
ncit:C7057
.
dgn-gda:DGNd8c307541e8a51ade9e772d93132610c
sio:SIO_000628
miriam-gene:3047
,
lld:C1868112
;
a
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.
}
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_provenance
{
dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_assertion
dcterms:description
"[Using gel retardation assays on various nuclear extracts, we also demonstrated that this novel mutation abolishes the binding of the ubiquitous CCAAT binding factor, CP1 to the distal CCAAT motif of the gamma-globin gene but does not affect the binding of any erythroid specific factor, thereby suggesting a possible role for CP1 in the developmental regulation of fetal globin expression.]. 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:1698280
;
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 .
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dgn-np:NP544809.RASvCO1OvPRHHfB7wLsbnmFnhL3buDSFsVFwOcmnPE7GI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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
<
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> , <
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
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