Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion wasGeneratedBy ECO_0000203 NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion wasDerivedFrom befree-20150227 NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion SIO_000772 9393760 NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion evidence source_evidence_literature NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.
- NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_assertion description "[We have determined the genomic organization and intron/exon boundaries of Hel-N1 and have screened the entire coding region for mutations by sequencing 14 primary SCLCs and cell lines and 21 primary NSCLCs preselected for localized 9p21 deletion or monosomy of chromosome 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP372964.RA9QdztMOOkzjSXinH3YFU1New_Mydswdrp4t1IjaKsyQ130_provenance.