Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion> ?p ?o ?g. }
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- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion type Assertion NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_head.
- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion description "[FOXP2 mutation causes a severe inherited speech and language defect, while the related transcription factors FOXP1, FOXP3 and FOXP4 are implicated in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_provenance.
- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion evidence source_evidence_literature NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_provenance.
- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion SIO_000772 20096010 NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_provenance.
- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion wasDerivedFrom befree-20150227 NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_provenance.
- NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_assertion wasGeneratedBy ECO_0000203 NP966009.RAEBdVpD_bk_NrDeI4HHcugFtWrQvd20czIJYVimS1MMc130_provenance.