Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion description "[To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with the varying expression of disorders in presented nevoid basal cell carcinoma syndrome (NBCCS) phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion evidence source_evidence_literature NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion SIO_000772 10554356 NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion wasDerivedFrom befree-2016 NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_assertion wasGeneratedBy ECO_0000203 NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.
- befree-2016 importedOn "2016-02-19" NP267255.RA0xfKEjSmf69tOZOlOXFTbhytzuGMfiYXOFFo1hV6pMA130_provenance.