@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o
> .
@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:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_head
{
this:
np:hasAssertion
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_assertion
;
np:hasProvenance
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_assertion
a
np:Assertion
.
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_provenance
a
np:Provenance
.
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_assertion
{
miriam-gene:2175
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN7ba698d3d7a241b46cba9ac61a39c4a7
sio:SIO_000628
miriam-gene:2175
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_provenance
{
dgn-np:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_assertion
dcterms:description
"[This may explain the observed lack of correlation between type of FANCA mutation and cellular phenotype or clinical severity in terms of age of onset of hematologic disease or number of malformations.]. 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:21273304
;
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:NP868298.RALETZpLsjf0rVL2QTyzsZhUFB1SXyEohIcTS1s1DXd5o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:18+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" .
}