Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- befree-2016 importedOn "2016-02-19" NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_assertion wasGeneratedBy ECO_0000203 NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_assertion wasDerivedFrom befree-2016 NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_assertion SIO_000772 17054105 NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_assertion evidence source_evidence_literature NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.
- NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_assertion description "[Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575418.RA79c2yw_7xLt-9Z3f6fils3bRbL2u-MguNT98r-2kjjw130_provenance.