Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_assertion description "[To define the defect of NTRK1 in CIPA patients, we have introduced one of the previously reported mutations (Gly571Arg) into both the NTRK1 and the TRK-T3 oncogene cDNAs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_assertion evidence source_evidence_literature NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_assertion SIO_000772 10567924 NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_assertion wasDerivedFrom befree-2016 NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_assertion wasGeneratedBy ECO_0000203 NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.
- befree-2016 importedOn "2016-02-19" NP268033.RAaUD4RJDitRTN2tORRv8VOQcge_mtWPVbd1MugHQdVT4130_provenance.