@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E
> .
@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:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_head
{
this:
np:hasAssertion
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion
;
np:hasProvenance
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance
;
np:hasPublicationInfo
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion
a
np:Assertion
.
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance
a
np:Provenance
.
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion
{
miriam-gene:3047
a
ncit:C16612
.
lld:C0472772
a
ncit:C7057
.
dgn-gda:DGN1914586a9a0d96a88f25dc4bb7dc2cd8
sio:SIO_000628
miriam-gene:3047
,
lld:C0472772
;
a
sio:SIO_001121
.
}
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_provenance
{
dgn-np:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_assertion
dcterms:description
"[Methodology suitable for such studies is reviewed, various abnormal fetal hemoglobins are discussed, the occurrence of Hb Bart's (gamma 4) and of the embryonic zeta chain is evaluated, and the various types of gamma-globin gene rearrangements (-A gamma.A gamma-; -G gamma.G gamma-; gamma-thalassemia; gamma-globin gene triplications, quadruplications, and quintuplications) are compared.]. 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:1802881
;
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:NP482256.RAGmvavPm9t-pgGVNgs4RMCcqQzQ4C_hNNzsr7bVxxy1E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}