Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion> ?p ?o ?g. }
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- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion type Assertion NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_head.
- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion wasGeneratedBy ECO_0000203 NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_provenance.
- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion wasDerivedFrom lhgdn-20090331 NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_provenance.
- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion SIO_000772 15001591 NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_provenance.
- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion evidence source_evidence_literature NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_provenance.
- NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_assertion description "[six novel and two recurrent intragenic KAL1 mutations in seven familial and four sporadic male cases of Kallmann syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152394.RA296gXNfPFmAtlPkhlL02t_V_Reh-d4C0kzxTUDpoceE130_provenance.