Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_assertion description "[ASXL1-MT mice displayed features of human-associated MDS, including multi-lineage myelodysplasia, pancytopenia, and occasional progression to overt leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_assertion evidence source_evidence_literature NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_assertion SIO_000772 24216483 NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_assertion wasDerivedFrom befree-20140225 NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_assertion wasGeneratedBy ECO_0000203 NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP182871.RALGvQ8DkFqmMs7CWOcoUe4pfjnkV4SQJgvZ77oBLF0hg130_provenance.