Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_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." NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_assertion evidence source_evidence_literature NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_assertion SIO_000772 22319038 NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_assertion wasDerivedFrom befree-20150227 NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_assertion wasGeneratedBy ECO_0000203 NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP936082.RA6kU0l8E6SpQH5XedPC8X9xiYCszl-OY4KTZ7YLtq00E130_provenance.