Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_assertion wasGeneratedBy ECO_0000203 NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_assertion wasDerivedFrom befree-20140225 NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_assertion SIO_000772 23297359 NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_assertion evidence source_evidence_literature NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_assertion description "[We subsequently sequenced CTSF in 22 unrelated individuals with suspected recessive Kufs disease, and identified an additional patient with compound heterozygous mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP560679.RAjFV2ksmN1U4yJ59HPjXtdRUmcFA8fg8cFtf1ZQgBt_s130_provenance.