Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion description "[In addition, another unreported heterozygous missense germline MEN1 mutation, Trp220Leu, was identified in an unrelated male patient with FIHP, whose mother and sister also had primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion evidence source_evidence_literature NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion SIO_000772 18084346 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion wasDerivedFrom befree-2016 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion wasGeneratedBy ECO_0000203 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- befree-2016 importedOn "2016-02-19" NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.