Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_assertion description "[The phenotype and allele frequencies of the four gene loci (AB0, RH, PTC and colour blindness) show considerable differences between these populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_assertion evidence source_evidence_literature NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_assertion SIO_000772 14524000 NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_assertion wasDerivedFrom befree-20150227 NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_assertion wasGeneratedBy ECO_0000203 NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP392629.RAfmgtXs5_CECPg2sG5sByhzdV4D5EJHWIXATo3yoLkO0130_provenance.