@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E
> .
@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:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_head
{
this:
np:hasAssertion
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_assertion
;
np:hasProvenance
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_provenance
;
np:hasPublicationInfo
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_assertion
a
np:Assertion
.
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_provenance
a
np:Provenance
.
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_assertion
{
miriam-gene:3039
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGNe48ede1dc32b096bb1dc93845df634f6
sio:SIO_000628
miriam-gene:3039
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_provenance
{
dgn-np:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_assertion
dcterms:description
"[Multiallelic DNA probes from within the alpha globin cluster were used to determine the number of copies of this locus in three cell lines containing trisomies of the short arm of chromosome 16 and one with a familial inversion, inv(16).]. 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:2879933
;
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:NP186038.RAj2wOhb1sppgMytC7bSlzNX_XjMwabACLUXcbyw3Zb5E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}