Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion description "[Here, we report two familial cases of LWD with a large Xp terminal deletion (approximately 943 kb) of distal PAR1 encompassing the SHOX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion evidence source_evidence_literature NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion SIO_000772 19400538 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion wasDerivedFrom befree-20140225 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_assertion wasGeneratedBy ECO_0000203 NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP544635.RAP7294KyoKwT7mO-8CissRAAylpoUp4N5DOXf9j6aStg130_provenance.