Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion description "[The gene mutated in families displaying the `incomplete phenotype` of CSNB (i.e., CSNB2) has recently been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion evidence source_evidence_literature NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion SIO_000772 10982042 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion wasDerivedFrom befree-20140225 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion wasGeneratedBy ECO_0000203 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.