Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_assertion description "[The most frequent p63 mutation syndrome is the EEC syndrome, characterized by ectrodactyly, ectodermal dysplasia and cleft lip/palate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_assertion evidence source_evidence_literature NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_assertion SIO_000772 23407076 NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_assertion wasDerivedFrom befree-20150227 NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_assertion wasGeneratedBy ECO_0000203 NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674885.RAbXhe7L9AsGVTI3PCjUYiHg5iNKK8RcK7f9RvbkDSHKg130_provenance.