Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_assertion description "[Our data support a model in which the hypopigmentation in WS, of which these factors have been implicated, results from a disruption in function of the central melanocyte transcription factor MITF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_assertion evidence source_evidence_literature NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_assertion SIO_000772 10982026 NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_assertion wasDerivedFrom befree-20150227 NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_assertion wasGeneratedBy ECO_0000203 NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557192.RA82Xp2TQIyjdbB9ECZLA_zdQ27FTFD8_ctM9LH0JHxbA130_provenance.