Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_assertion description "[In addition, we found an even wider spectrum of reproductive function within pedigrees carrying an FGFR1 mutation ranging from IHH to delayed puberty to normal reproductive function (anosmia only or asymptomatic carriers).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_assertion evidence source_evidence_literature NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_assertion SIO_000772 16764984 NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_assertion wasDerivedFrom befree-20150227 NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_assertion wasGeneratedBy ECO_0000203 NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400161.RA91EJjC7vY4Ktk6qFF10jtiZeltRerbkD9oSEsswMZMo130_provenance.