Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_assertion description "[Rare point mutation at codon 301 and 969 of FMS/M-CSF receptor in acute myelomonocytic and monocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_assertion evidence source_evidence_literature NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_assertion SIO_000772 1385636 NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_assertion wasDerivedFrom befree-2016 NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_assertion wasGeneratedBy ECO_0000203 NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.
- befree-2016 importedOn "2016-02-19" NP412801.RAAAjErlTXNDnF5HE6-ns1mVzutfu0R--sdc_qAKwG0Bc130_provenance.