Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_assertion description "[Heterozygous mutations in p63 are associated with split hand/foot malformations (SHFM), orofacial clefting, and ectodermal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_assertion evidence source_evidence_literature NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_assertion SIO_000772 20808887 NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_assertion wasDerivedFrom befree-20140225 NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_assertion wasGeneratedBy ECO_0000203 NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP611867.RASYNbxnNtD6MgTOzswAKuhj9efZ4sXI_qcRHidhWD_dA130_provenance.