Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_assertion wasGeneratedBy ECO_0000203 NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_assertion wasDerivedFrom gad-20150221 NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_assertion SIO_000772 15001591 NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_assertion evidence source_evidence_literature NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.
- NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_assertion description "[Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78762.RAKXUfJM1D5nsOs4y1Lg1qpTSrqdKy4izleWzSgm1Jodg130_provenance.