Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion wasGeneratedBy ECO_0000203 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion wasDerivedFrom befree-20150227 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion SIO_000772 23171239 NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion evidence source_evidence_literature NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.