@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk
> .
@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/v3.0.0/void/
> .
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_head
{
this:
np:hasAssertion
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion
;
np:hasProvenance
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion
a
np:Assertion
.
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance
a
np:Provenance
.
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion
{
miriam-gene:6926
a
ncit:C16612
.
lld:C1866994
a
ncit:C7057
.
dgn-gda:DGN92676a8a32e9bfce0fdee4a7b52d2e52
sio:SIO_000628
miriam-gene:6926
,
lld:C1866994
;
a
sio:SIO_001121
.
}
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_provenance
{
dgn-np:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_assertion
dcterms:description
"[Ulnar mammary syndrome (UMS), an autosomal dominant disorder caused by mutations in TBX3, underscores the importance of TBX3 in human breast development, while abnormal mammary gland development in Tbx2 or Tbx3 mutant mice provides models for experimental investigation.]. 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:23624936
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP724661.RAwgnABK04kN3eFQBmAAFobHe9n8YGlIG4cX62ip0_DHk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:57+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}