Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_assertion description "[Mutation analysis using sequencing of RT-PCR products and Northern blot analysis in MKS patients exclude PNUTL2 as the gene for MKS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_assertion evidence source_evidence_literature NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_assertion SIO_000772 9889007 NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_assertion wasDerivedFrom befree-20140225 NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_assertion wasGeneratedBy ECO_0000203 NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP707279.RAtIPeZDlr0spADZ8_wUiqPHqjRsMuDVRu2Hg5owvPZkY130_provenance.