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- source_evidence_literature type ECO_0000212 NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- befree-2016 importedOn "2016-02-19" NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_assertion wasGeneratedBy ECO_0000203 NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_assertion wasDerivedFrom befree-2016 NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_assertion SIO_000772 20375215 NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_assertion evidence source_evidence_literature NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.
- NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_assertion description "[Deletions spanning or surrounding the SHOX gene account for a significant proportion of patients with idiopathic short stature (ISS) and allied disorders, such as Leri-Weill dyschondrosteosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804805.RAzn4Wx_QptCJyAUJXm0YBSU8_H6fKS79TJ-u3iAu3l3s130_provenance.