Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_assertion description "[Fifteen novel ALPL mutations have been found in a series of 11 families from various origins affected by perinatal and infantile hypophosphatasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_assertion evidence source_evidence_literature NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_assertion SIO_000772 12815606 NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_assertion wasDerivedFrom lhgdn-20090331 NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_assertion wasGeneratedBy ECO_0000203 NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP151465.RAfwZx49WrPwjixWPViORXySmq_z0Hfl6MM0fXC52BiGg130_provenance.