Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion> ?p ?o ?g. }
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- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion type Assertion NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_head.
- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion description "[A total of 103 patients with either CPHD (n = 35) or SOD (n = 68) were investigated for mutations in genes implicated in the etiology of KS (FGFR1, FGF8, PROKR2, PROK2, and KAL1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_provenance.
- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion evidence source_evidence_literature NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_provenance.
- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion SIO_000772 22319038 NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_provenance.
- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion wasDerivedFrom befree-20150227 NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_provenance.
- NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_assertion wasGeneratedBy ECO_0000203 NP520897.RAH4xBlk3KFr_AMUE7-VxD2NZf9XUdf1D0LsB92g_PKpw130_provenance.