Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_assertion description "[These data provide a proof-of-concept that the catalogue of p63 binding sites identified in this study may be of relevance to the studies of SHFM and other congenital malformations that resemble the p63-associated phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_assertion evidence source_evidence_literature NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_assertion SIO_000772 20808887 NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_assertion wasDerivedFrom befree-20150227 NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_assertion wasGeneratedBy ECO_0000203 NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.
- befree-20150227 importedOn "2015-02-27" NP799396.RA9ecF0G2oL4ZD8Pw3ZlS4_ozLpo6gHF-yafTHwZGwu90130_provenance.