Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_assertion description "[Our observation increases the number of cases with fibulin-4 mutations to three and extends the phenotypic spectrum of fibulin-4 mutations by microcephaly, overgrowth and arachnodactyly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_assertion evidence source_evidence_literature NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_assertion SIO_000772 19664000 NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_assertion wasDerivedFrom befree-2016 NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_assertion wasGeneratedBy ECO_0000203 NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.
- befree-2016 importedOn "2016-02-19" NP756111.RAwVIpYuH__O8A0OF-68lhoXKpDtnwkQb_jDs1MklEgkE130_provenance.