@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw
> .
@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:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_head
{
this:
np:hasAssertion
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_assertion
;
np:hasProvenance
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_assertion
a
np:Assertion
.
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_provenance
a
np:Provenance
.
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNd988dc676bf14121855dd53c4e2036ca
sio:SIO_000628
miriam-gene:1813
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_provenance
{
dgn-np:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_assertion
dcterms:description
"[Although IBF had high dopamine D2 receptor affinity, its ability to detect melanoma metastases is more likely explained by low affinity binding to melanin than by the presence of dopamine receptors.]. 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:8944340
;
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:NP766469.RA-4lftdoLkztqhRZNIz-y2uV_OtnvdCCcxXNJoXImcFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}