Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion> ?p ?o ?g. }
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- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion type Assertion NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_head.
- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion description "[We performed p63 mutation analysis in a sample of 43 individuals and families affected with EEC syndrome, in 35 individuals affected with SHFM, and in three families with the EEC-like condition limb-mammary syndrome (LMS), which is characterized by ectrodactyly, cleft palate, and mammary-gland abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_provenance.
- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion evidence source_evidence_literature NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_provenance.
- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion SIO_000772 11462173 NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_provenance.
- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion wasDerivedFrom befree-2016 NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_provenance.
- NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_assertion wasGeneratedBy ECO_0000203 NP324426.RA4qVDOOwxgAs50Z-XT-M5O5uAaKDz2k9pfs8Ir0w3YSk130_provenance.