Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_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." NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_assertion evidence source_evidence_literature NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_assertion SIO_000772 16690726 NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_assertion wasDerivedFrom befree-2016 NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_assertion wasGeneratedBy ECO_0000203 NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.
- befree-2016 importedOn "2016-02-19" NP549304.RAdnnCKecqAkh5jdk014PhcpvwEneIBRFrJttXZC3hBT0130_provenance.