Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_assertion description "[Mutations in the p63 gene are found in a number of human syndromes, including ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) syndrome, limb-mammary syndrome (LMS), Hay-Wells syndrome and in non-syndromic split-hand/split-foot malformation (SHFM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_assertion evidence source_evidence_literature NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_assertion SIO_000772 11929852 NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_assertion wasDerivedFrom befree-2016 NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_assertion wasGeneratedBy ECO_0000203 NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.
- befree-2016 importedOn "2016-02-19" NP350575.RAkPYZxv8EkPWmlWMGp2YNoSCGm7Ln1OPusvu6LOxgIpY130_provenance.