@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI
> .
@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:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_head
{
this:
np:hasAssertion
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion
;
np:hasProvenance
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion
a
np:Assertion
.
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance
a
np:Provenance
.
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion
{
miriam-gene:5077
a
ncit:C16612
.
lld:C3266898
a
ncit:C7057
.
dgn-gda:DGNf29ab81dd127a7b0d63acd5031e3fe94
sio:SIO_000628
miriam-gene:5077
,
lld:C3266898
;
a
sio:SIO_001121
.
}
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_provenance
{
dgn-np:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_assertion
dcterms:description
"[The structure elucidates the role of serine 50 in selection of the CG sequence immediately 3' of the TAAT motif by PAX class homeodomains and provides insights into the molecular mechanisms by which certain Waardenburg syndrome-associated missense mutations could destabilize the fold of the PAX3 homeodomain whereas others could affect its interaction with DNA.]. 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:19199574
;
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:NP401954.RALBvVWx2WvtP0Db9MyHs-Km3fgWlwQ38Mp8JkiS3zUTI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}