Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_assertion description "[Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_assertion evidence source_evidence_literature NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_assertion SIO_000772 19206169 NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_assertion wasDerivedFrom gad-20150221 NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_assertion wasGeneratedBy ECO_0000203 NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123923.RAHaZh5F5BIL4RUBUNviuAZYZDK0JXEfwZQYLP37e-HUM130_provenance.