@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc
> .
@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:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_head
{
this:
np:hasAssertion
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_assertion
;
np:hasProvenance
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_assertion
a
np:Assertion
.
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_provenance
a
np:Provenance
.
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_assertion
{
miriam-gene:2175
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN1905757a9c98633e7ca815776fb09923
sio:SIO_000628
miriam-gene:2175
,
lld:C0018939
;
a
sio:SIO_001121
.
}
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_provenance
{
dgn-np:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_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:NP868301.RAk3ZqwU1mKpfrQ74xiOd4VSSy_HO1Ppt95ePbbObYDUc130_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" .
}