Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_assertion description "[Recently, LSP1 was identified as the 47-kD protein overexpressed in the polymorphonuclear neutrophils of patients with a rare neutrophil disorder, neutrophil actin dysfunction with abnormalities of 47-kD and 89-kD proteins (NAD 47/89).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_assertion evidence source_evidence_literature NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_assertion SIO_000772 9616178 NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_assertion wasDerivedFrom befree-20140225 NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_assertion wasGeneratedBy ECO_0000203 NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846401.RAbjjVP-5V362fjDGBFQCn5uPjSDtxmlARr6P-eUyjn48130_provenance.