Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion description "[Loss-of-function mutations in KIND1 and KIND3 cause Kindler syndrome and leukocyte adhesion deficiency-III syndrome, respectively, although no human disease has yet been associated with KIND2 gene pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion evidence source_evidence_literature NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion SIO_000772 19854292 NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion wasDerivedFrom befree-2016 NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_assertion wasGeneratedBy ECO_0000203 NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.
- befree-2016 importedOn "2016-02-19" NP771462.RAm_ElcflHm2AKB4Bg1wSHXnQvn6MBZSknuws2eRPC2Q0130_provenance.