Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion> ?p ?o ?g. }
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- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion type Assertion NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_head.
- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion description "[If no causative ENG or ACVRL1 mutation is found, proband samples are referred for sequence analysis of MADH4 (associated with a combined syndrome of juvenile polyposis and HHT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_provenance.
- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion evidence source_evidence_literature NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_provenance.
- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion SIO_000772 16690726 NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_provenance.
- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion wasDerivedFrom befree-2016 NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_provenance.
- NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_assertion wasGeneratedBy ECO_0000203 NP549303.RAWrDiRSxucc6sSfyGzrfn_ObZ_PLuGXsz4y2r4fhT_Cc130_provenance.