Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_assertion description "[We find from a literature review that missense mutations within the FNIII domain of MID1 are associated with a milder presentation of OS than missense mutations elsewhere in MID1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_assertion evidence source_evidence_literature NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_assertion SIO_000772 16378742 NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_assertion wasDerivedFrom befree-2016 NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_assertion wasGeneratedBy ECO_0000203 NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.
- befree-2016 importedOn "2016-02-19" NP528459.RAcb99CfK9shSEePn87coJMFHnT1ySA6Vg92sNVjLbVbc130_provenance.