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- source_evidence_literature type ECO_0000212 NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_assertion description "[A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple caf�-au-lait spots.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_assertion evidence source_evidence_literature NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_assertion SIO_000772 11809679 NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_assertion wasDerivedFrom befree-20150227 NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_assertion wasGeneratedBy ECO_0000203 NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP570111.RAMWBwtlDlruCO-oMtgQiIMi3grq3fPnOJLA92IC9m_LE130_provenance.