Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_assertion description "[This suggests that the corresponding human GRB10 Type I plays an important role in the etiology of Silver-Russell syndrome caused by partial trisomy of 7p11-p13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_assertion evidence source_evidence_literature NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_assertion SIO_000772 19174477 NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_assertion wasDerivedFrom befree-20140225 NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_assertion wasGeneratedBy ECO_0000203 NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690236.RAvkL_vWFSaw_nJfRTNzNa9ROiAQj9E5aYylIKybsWo1Q130_provenance.